510(k) K821537 ยท FMF Syringe, Piston
HENKE DISPOSABLE SYRINGE
| Applicant | C. B. Dumont Company, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 28, 1982 |
| Received | May 24, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821537
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 27, 2023 | Wolf, Henke Sass, Gmbh Henke-Ject-2 part luer sterile single use syringes - used for intravenous, intramuscular, subcutaneous, intracutaneous and intraarterial injection of liquids or diluted drugs in combination with an ad Open, Classified |
FMF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.