510(k) K973620 ยท FMI Needle, Hypodermic, Single Lumen
VACUETTE MULTI-SAMPLE NEEDLE
| Applicant | Greiner Meditech, Inc., Bel Air MD, US |
| Decision | Substantially Equivalent, Dec 17, 1997 |
| Received | Sep 23, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973620
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.