510(k) K903878 ยท HQQ Apparatus, Cautery, Radiofrequency, Battery-Powered
MENTOR(R) DURASTAT(TM) AUTOCLAV BIPOLAR HEMOSTAT
| Applicant | Mentor O & O, Inc., Norwell MA, US |
| Decision | Substantially Equivalent, Nov 5, 1990 |
| Received | Aug 22, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903878
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.