N-S Medical Products: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “N-S Medical Products” (first 1987, latest 1988), across 3 product codes in 2 review panels. Median 510(k) review time under this name: 31 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 |
|---|---|---|---|
| DQX | Wire, Guide, Catheter | 2 | 2 |
| KNW | Instrument, Biopsy | 2 | 2 |
| GDM | Needle, Aspiration And Injection, Reusable | 1 | 1 |
Review panels
Most recent N-S Medical Products 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K880288 | TRU-TRAC TORQUE GUIDEWIRE | DQX | 1988-09-12 | 231 |
| K880287 | TRU-TRAC COILED GUIDEWIRE | DQX | 1988-09-12 | 231 |
| K881957 | HAWKINS-AKINS BLUNT NEEDLE ACCESS KIT | KNW | 1988-05-20 | 10 |
| K881956 | NATIONAL-STANDARD NEEDLE HOLDER | KNW | 1988-05-20 | 10 |
| K870523 | HAWKINS BREAST LOCALIZATION NEEDLE | GDM | 1987-03-09 | 31 |
Recalls
openFDA lists no recalls under a recalling firm named N-S Medical Products.
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 N-S Medical Products?
FDA lists 5 510(k) clearances under the applicant name “N-S Medical Products” (first 1987, latest 1988), across 3 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 N-S Medical Products?
The median time from FDA receipt to decision across 510(k)s cleared under the name N-S Medical Products is 31 days.
Which FDA product codes appear under N-S Medical Products?
The most frequent FDA product codes under this applicant name are DQX (Wire, Guide, Catheter, 2); KNW (Instrument, Biopsy, 2); GDM (Needle, Aspiration And Injection, Reusable, 1).
Next steps
- See all 5 N-S Medical Products clearances with predicates and recalls
- Run predicate analysis for product code DQX, N-S Medical Products'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.