510(k) K863570 ยท KGS Retention Device, Suture
LE VEEN WOUND SPLINT
| Applicant | Tek-Aid, Inc., Charleston SC, US |
| Decision | Substantially Equivalent, Sep 29, 1986 |
| Received | Sep 12, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863570
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.