510(k) K933324 ยท MJG Device, Percutaneous, Biopsy
SKIN BIOPSY DEVICE
| Applicant | Nhr, Inc., Monroe MI, US |
| Decision | Substantially Equivalent, Mar 31, 1994 |
| Received | Jul 12, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933324
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.