510(k) K803199 ยท KDD Kit, Surgical Instrument, Disposable
SUTURE REMOVAL KIT
| Applicant | Walpak Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 15, 1981 |
| Received | Dec 17, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K803199
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.