510(k) K911397 ยท FCG Biopsy Needle
HYPODERMIC NEEDLES, SINGLE LUMEN
| Applicant | Popper & Sons, Inc., New Hyde Park NY, US |
| Decision | Substantially Equivalent, May 20, 1991 |
| Received | Mar 29, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911397
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.