510(k) K964827 ยท MCZ Suture Removal Kit
PROD. NO. 01-132 - SUTURE REMOVAL KIT
| Applicant | Continental Medical Laboratories, Inc., Waterford WI, US |
| Decision | Substantially Equivalent, Feb 14, 1997 |
| Received | Dec 2, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964827
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.