Windsor Medical, Inc.: FDA filings under this applicant name
FDA lists 9 510(k) clearances under the applicant name “Windsor Medical, Inc.” (first 1983, latest 1984), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 61 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 |
|---|---|---|---|
| FRN | Pump, Infusion | 8 | 8 |
| FRW | Scale, Patient | 1 | 1 |
Review panels
- General Hospital (9)
Most recent Windsor Medical, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K841481 | WINDSOR MEDICAL MODEL 50-00002 | FRN | 1984-05-21 | 42 |
| K832606 | WINDSOR MEDICAL VARIOUS MODELS | FRN | 1983-11-29 | 118 |
| K832641 | WINDSOR MEDICAL MODEL 52 | FRN | 1983-10-04 | 61 |
| K830657 | AMBULATORY MARK XI DRUG INFUSION DEV- | FRN | 1983-09-16 | 198 |
| K830656 | AMBULATORY MARK III INFUSION DEVICE | FRN | 1983-08-16 | 167 |
| K830544 | WINDSOR MEDICAL, INC. 50-01-028 | FRN | 1983-03-31 | 37 |
| K830490 | MODEL 50-01-27 | FRN | 1983-03-31 | 44 |
| K830317 | INFUSION PUMP ACCESS. #60-01-5 | FRW | 1983-03-31 | 59 |
| K822842 | AMBULATORY MARK I | FRN | 1983-03-24 | 182 |
Recalls
openFDA lists no recalls under a recalling firm named Windsor Medical, 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.
Related HCPCS codes
HCPCS Level II codes whose descriptors match the device names of the product codes filed under Windsor Medical, Inc. (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)
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.
- Windsor Laboratories, Inc. (19 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Windsor Medical, Inc.?
FDA lists 9 510(k) clearances under the applicant name “Windsor Medical, Inc.” (first 1983, latest 1984), across 2 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Windsor Medical, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Windsor Medical, Inc. is 61 days.
Which FDA product codes appear under Windsor Medical, Inc.?
The most frequent FDA product codes under this applicant name are FRN (Pump, Infusion, 8); FRW (Scale, Patient, 1).
Next steps
- See all 9 Windsor Medical, Inc. clearances with predicates and recalls
- Run predicate analysis for product code FRN, Windsor Medical, 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.