510(k) K942818 ยท MDM Instrument, Manual, Surgical, General Use
DEEP SUTURE
| Applicant | Automated Medical Products Corp., New York NY, US |
| Decision | Substantially Equivalent, Aug 25, 1994 |
| Received | Jun 15, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942818
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.