510(k) K832138 ยท KGS Retention Device, Suture
BIOMER * PLEDGET SUTURE BUTTRESS
| Applicant | ETHICON, Inc., Walker MI, US |
| Decision | Substantially Equivalent, May 23, 1984 |
| Received | Jul 1, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832138
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.