510(k) K922919 ยท MJG Device, Percutaneous, Biopsy
DYNACYT BIOPSY ASPIRATION DEVICE
| Applicant | Buckman Co., Inc., Concord CA, US |
| Decision | Substantially Equivalent, Mar 31, 1993 |
| Received | Jun 17, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922919
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.