Chesebrough-Pond'S U.S.A. Co.: FDA filings under this applicant name
FDA lists 33 510(k) clearances under the applicant name “Chesebrough-Pond'S U.S.A. Co.” (first 1976, latest 1987), across 19 product codes in 5 review panels. Median 510(k) review time under this name: 52 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| NAD | Dressing, Wound, Occlusive | 5 | 5 |
| KNT | Tubes, Gastrointestinal (And Accessories) | 4 | 4 |
| BWF | Spirometer, Therapeutic (Incentive) | 3 | 3 |
| FRO | Dressing, Wound, Drug | 3 | 3 |
| KNX | Collector, Urine, (And Accessories) For Indwelling Catheter | 3 | 3 |
| EFQ | Gauze/Sponge, Internal | 2 | 2 |
| BZG | Spirometer, Diagnostic | 1 | 1 |
| BZK | Spirometer, Monitoring (W/Wo Alarm) | 1 | 1 |
| CAF | Nebulizer (Direct Patient Interface) | 1 | 1 |
| CBP | Valve, Non-Rebreathing | 1 | 1 |
Plus 9 more product codes.
Review panels
- General and Plastic Surgery (11)
- Anesthesiology (8)
- Gastroenterology and Urology (8)
- General Hospital (5)
- Ear, Nose and Throat (1)
Most recent Chesebrough-Pond'S U.S.A. Co. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K863866 | RESPIRADYNE II(TM) | BZK | 1987-01-28 | 117 |
| K862803 | CHESEBROUGH POND'S HYDROCOLLOID DRESSING | FRO | 1986-11-14 | 115 |
| K851383 | BLISTERFILM TRANSPARENT DRESSING | NAD | 1985-07-05 | 88 |
| K851382 | CHESEBROUGH-POND'S SEQUENTIAL WOUND DRESSING | NAD | 1985-07-05 | 88 |
| K851539 | CHESEBROUGH-PONDS KANGAROO PUMP SET W/EASY-CAP CLO | KNT | 1985-06-12 | 57 |
| K843567 | KANGAROO NASOGASTRIC FEEDING TUBE | KNT | 1985-02-14 | 157 |
| K845010 | CHESEBROUGH-POND'S URI-DRAIN MALE URINARY POUCH | EYQ | 1985-01-15 | 20 |
| K844186 | CONTINENT STOMA SYSTEM & ACCESSORIES | KBG | 1985-01-15 | 78 |
| K844789 | KANGAROO ACCESS II ENTERAL FEEDING CONTAINER | KNT | 1985-01-02 | 23 |
| K843128 | FEMALE URINARY INCONTINENCE SYS | KNX | 1985-01-02 | 146 |
23 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Chesebrough-Pond'S U.S.A. Co..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Related HCPCS codes
HCPCS Level II codes whose descriptors match the device names of the product codes filed under Chesebrough-Pond'S U.S.A. Co. (a text match, not an official crosswalk):
- A4220 — Refill kit for implantable infusion pump (via FRN)
- E0786 — Implantable programmable infusion pump, replacement (excludes implantable intraspinal catheter) (via FRN)
- E0785 — Implantable intraspinal (epidural/intrathecal) catheter used with implantable infusion pump, replacement (via FRN)
- G0379 — Direct admission of patient for hospital observation care (via CAF)
Frequently asked questions
How many FDA 510(k) clearances are listed under Chesebrough-Pond'S U.S.A. Co.?
FDA lists 33 510(k) clearances under the applicant name “Chesebrough-Pond'S U.S.A. Co.” (first 1976, latest 1987), across 19 product codes in 5 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Chesebrough-Pond'S U.S.A. Co.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Chesebrough-Pond'S U.S.A. Co. is 52 days.
Which FDA product codes appear under Chesebrough-Pond'S U.S.A. Co.?
The most frequent FDA product codes under this applicant name are NAD (Dressing, Wound, Occlusive, 5); KNT (Tubes, Gastrointestinal (And Accessories), 4); BWF (Spirometer, Therapeutic (Incentive), 3).
Next steps
- See all 33 Chesebrough-Pond'S U.S.A. Co. clearances with predicates and recalls
- Run predicate analysis for product code NAD, Chesebrough-Pond'S U.S.A. Co.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.