510(k) K000212 ยท KOH Instrument, Manual, General Obstetric-Gynecologic
KSEA CHARDONNES MORCELLATION KNIFE
| Applicant | KARL STORZ Endoscopy-America, Inc., Culver City CA, US |
| Decision | Substantially Equivalent, Apr 21, 2000 |
| Received | Jan 24, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000212
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.