The Kipp Group: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “The Kipp Group” (first 1997, latest 2000), across 1 product code in 1 review panel. Median 510(k) review time under this name: 56 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 |
|---|---|---|---|
| FPA | Set, Administration, Intravascular | 6 | 6 |
Review panels
- General Hospital (6)
Most recent The Kipp Group 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K000343 | NAC Y-ADP | FPA | 2000-03-01 | 27 |
| K000152 | KIPPMED I.V. MANIFOLD | FPA | 2000-02-29 | 41 |
| K993147 | DECAP | FPA | 1999-11-02 | 42 |
| K992268 | NAC PRN NEEDLELESS ACCESS CONNECTOR | FPA | 1999-09-15 | 71 |
| K991932 | INTRAVASCULAR ADMINISTRATION SET | FPA | 1999-08-20 | 73 |
| K970255 | KIPP MED I.V. MANIFOLD | FPA | 1997-04-14 | 82 |
Recalls
openFDA lists no recalls under a recalling firm named The Kipp Group.
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 The Kipp Group?
FDA lists 6 510(k) clearances under the applicant name “The Kipp Group” (first 1997, latest 2000), across 1 product code 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 The Kipp Group?
The median time from FDA receipt to decision across 510(k)s cleared under the name The Kipp Group is 56 days.
Which FDA product codes appear under The Kipp Group?
The most frequent FDA product codes under this applicant name are FPA (Set, Administration, Intravascular, 6).
Next steps
- See all 6 The Kipp Group clearances with predicates and recalls
- Run predicate analysis for product code FPA, The Kipp Group'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.