510(k) K911448 ยท FCK Instrument, Biopsy, Suction
MULTIPLE BIOPSY DEVICE-MBX
| Applicant | Triton Technology, Inc., Salem OH, US |
| Decision | Substantially Equivalent, Apr 16, 1991 |
| Received | Mar 15, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911448
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.