510(k) K926126 ยท MDM Instrument, Manual, Surgical, General Use
SUTUREMATE
| Applicant | Surgical Safety Products, Inc., Great Neck NY, US |
| Decision | Substantially Equivalent, May 19, 1993 |
| Received | Dec 4, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926126
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.