510(k) K932142 ยท FCK Instrument, Biopsy, Suction
SUCTION GUILLOTINE DEVICE
| Applicant | Triton Technology, Inc., Salem OH, US |
| Decision | Substantially Equivalent, Sep 24, 1993 |
| Received | May 3, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932142
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.