Consolidated Products & Services, Inc.: FDA filings under this applicant name
FDA lists 7 510(k) clearances under the applicant name “Consolidated Products & Services, Inc.” (first 1989, latest 1997), across 4 product codes in 3 review panels. Median 510(k) review time under this name: 18 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 |
|---|---|---|---|
| IMD | Pack, Hot Or Cold, Disposable | 3 | 3 |
| KNX | Collector, Urine, (And Accessories) For Indwelling Catheter | 2 | 2 |
| FPY | Sheet, Burn | 1 | 1 |
| KNT | Tubes, Gastrointestinal (And Accessories) | 1 | 1 |
Review panels
Most recent Consolidated Products & Services, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K974190 | CP&S INSTANT COLD PACK LIMB KIT TRANSPORTER | IMD | 1997-11-19 | 15 |
| K930759 | CP & S STERILE BURN SHEET | FPY | 1994-01-21 | 343 |
| K890551 | URINARY DRAINAGE UNIT | KNX | 1989-02-28 | 22 |
| K890550 | CP&S DISPOSABLE URINARY LEGBAG (MEDIUM & LARGE) | KNX | 1989-02-28 | 22 |
| K890552 | CP&S GAVAGE CONSTAINER, DISPOSABLE | KNT | 1989-02-24 | 18 |
| K890554 | CP&S DISPOSABLE INSTANT SUPER HOT COMPRESS | IMD | 1989-02-13 | 7 |
| K890553 | CP&S DISPOSABLE INSTANT COLD COMPRESS | IMD | 1989-02-13 | 7 |
Recalls
openFDA lists no recalls under a recalling firm named Consolidated Products & Services, Inc..
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.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Consolidated Technologies, Inc. (20 510(k)s)
- Consolidated Medical Equipment, Inc. (15 510(k)s)
- Consolidated Technology (4 510(k)s)
- Consolidated Machine Corp. (2 510(k)s)
- Consolidated Research of Richmond, Inc. (2 510(k)s)
- Consolidated Stores Corp. (2 510(k)s)
- Consolidated Technologies of Wisconsin (2 510(k)s)
- Consolidated Health & Sports Prod. (1 510(k)s)
- Consolidated Industries of Greater Syracuse, Inc. (1 510(k)s)
- Consolidated Medical Technologies (1 510(k)s)
- Consolidated Radiation Services, Inc. (1 510(k)s)
- Consolidated Research of Richmond, Inc. Dba General Sleep CO (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Consolidated Products & Services, Inc.?
FDA lists 7 510(k) clearances under the applicant name “Consolidated Products & Services, Inc.” (first 1989, latest 1997), across 4 product codes in 3 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 Consolidated Products & Services, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Consolidated Products & Services, Inc. is 18 days.
Which FDA product codes appear under Consolidated Products & Services, Inc.?
The most frequent FDA product codes under this applicant name are IMD (Pack, Hot Or Cold, Disposable, 3); KNX (Collector, Urine, (And Accessories) For Indwelling Catheter, 2); FPY (Sheet, Burn, 1).
Next steps
- See all 7 Consolidated Products & Services, Inc. clearances with predicates and recalls
- Run predicate analysis for product code IMD, Consolidated Products & Services, Inc.'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.