510(k) K000455 ยท FMI Needle, Hypodermic, Single Lumen
GETTIG GUARD
| Applicant | Gettig Pharmaceutical Instrument Co., Great Neck NY, US |
| Decision | Substantially Equivalent, Apr 19, 2000 |
| Received | Feb 11, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000455
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.