Northgate Research, Inc.: FDA filings under this applicant name
FDA lists 8 510(k) clearances under the applicant name “Northgate Research, Inc.” (first 1980, latest 1990), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 46 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 |
|---|---|---|---|
| FFK | Lithotriptor, Electro-Hydraulic | 5 | 5 |
| FGO | Dislodger, Stone, Flexible | 2 | 2 |
| FFL | Dislodger, Stone, Basket, Ureteral, Metal | 1 | 1 |
Review panels
Most recent Northgate Research, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K903337 | 1.9 FRENCH LITHOTRIPTER ELECTRODE | FFK | 1990-11-16 | 114 |
| K894704 | 2.5 FRENCH LITHOTRIPTOR ELECTRODE | FFK | 1989-10-18 | 85 |
| K891254 | UROLOGICAL STONE BASKET | FFL | 1989-03-22 | 14 |
| K891253 | UROLOGICAL GRASPING FORCEPS | FGO | 1989-03-22 | 14 |
| K891252 | UROLOGICAL LOOP RETRIEVERS | FGO | 1989-03-22 | 14 |
| K864904 | 3F ELECTRODE | FFK | 1987-02-10 | 57 |
| K852874 | 5F ELECTRODE(LITHOTRIPTOR) | FFK | 1985-08-21 | 44 |
| K802322 | MODEL SD-1 DISINTEGRATOR | FFK | 1980-11-10 | 48 |
Recalls
openFDA lists no recalls under a recalling firm named Northgate Research, 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.
- Northgate Technologies, Inc. (55 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Northgate Research, Inc.?
FDA lists 8 510(k) clearances under the applicant name “Northgate Research, Inc.” (first 1980, latest 1990), across 3 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 Northgate Research, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Northgate Research, Inc. is 46 days.
Which FDA product codes appear under Northgate Research, Inc.?
The most frequent FDA product codes under this applicant name are FFK (Lithotriptor, Electro-Hydraulic, 5); FGO (Dislodger, Stone, Flexible, 2); FFL (Dislodger, Stone, Basket, Ureteral, Metal, 1).
Next steps
- See all 8 Northgate Research, Inc. clearances with predicates and recalls
- Run predicate analysis for product code FFK, Northgate Research, 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.