510(k) K821502 ยท KDD Kit, Surgical Instrument, Disposable
STERILE SUTURE REMOVAL KIT
| Applicant | Pro-Pak, Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 9, 1982 |
| Received | May 19, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821502
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.