510(k) K925870 ยท MJG Device, Percutaneous, Biopsy
SPACER
| Applicant | Bip USA, Inc., Niagara Falls NY, US |
| Decision | Substantially Equivalent, May 19, 1993 |
| Received | Nov 19, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925870
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.