510(k) K923840 ยท GDF Guide, Needle, Surgical
NEEDLE-GRABBER
| Applicant | Guardian Angel Products, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jul 13, 1993 |
| Received | Jul 31, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923840
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.