Bissell Medical Products, Inc.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Bissell Medical Products, Inc.” (first 1985, latest 1995), across 2 product codes in 2 review panels. Median 510(k) review time under this name: 90 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 |
|---|---|---|---|
| KNT | Tubes, Gastrointestinal (And Accessories) | 5 | 5 |
| FPP | Stretcher, Hand-Carried | 1 | 1 |
Review panels
Most recent Bissell Medical Products, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K932880 | GRASSI GASTROJEJUNOSTOMY TUBE | KNT | 1995-06-07 | 723 |
| K914140 | GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEED | FPP | 1992-03-31 | 197 |
| K901683 | IMPROVED BAKER TWIN-CUFF SUMP TUBE | KNT | 1990-06-27 | 78 |
| K873441 | BAKER TWIN-CUFF INTESTINAL DECOMP/PLICATION TUBE | KNT | 1987-10-27 | 61 |
| K871691 | MODIFIED MULTI-LUMEN NASOGASTRIC TUBE | KNT | 1987-08-10 | 103 |
| K851672 | NYHUS/NELSON TUBE | KNT | 1985-07-09 | 77 |
Recalls
openFDA lists no recalls under a recalling firm named Bissell Medical Products, 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.
Frequently asked questions
How many FDA 510(k) clearances are listed under Bissell Medical Products, Inc.?
FDA lists 6 510(k) clearances under the applicant name “Bissell Medical Products, Inc.” (first 1985, latest 1995), across 2 product codes in 2 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 Bissell Medical Products, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Bissell Medical Products, Inc. is 90 days.
Which FDA product codes appear under Bissell Medical Products, Inc.?
The most frequent FDA product codes under this applicant name are KNT (Tubes, Gastrointestinal (And Accessories), 5); FPP (Stretcher, Hand-Carried, 1).
Next steps
- See all 6 Bissell Medical Products, Inc. clearances with predicates and recalls
- Run predicate analysis for product code KNT, Bissell Medical Products, 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.