510(k) K982439 ยท MKY System, Skin Closure
PROXIDERM, MODELS TN 460, TN 90 460, BK 460
| Applicant | Progressive Surgical Products, Inc., Westbury NY, US |
| Decision | Substantially Equivalent, Sep 8, 1998 |
| Received | Jul 14, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982439
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.