510(k) K904435 ยท KGS Retention Device, Suture
VENTROFIL TENSION RELIEF SUTURE SET
| Applicant | Aesculap, Inc., Burlingame CA, US |
| Decision | Substantially Equivalent, Aug 29, 1991 |
| Received | Sep 28, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904435
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.