510(k) K761193 ยท KDD Kit, Surgical Instrument, Disposable
SUTURE REMOVAL KIT
| Applicant | Superior Plastic Products Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 12, 1977 |
| Received | Dec 6, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K761193
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 11, 2013 | Covidien LLC Curity Staple Remover Kit; Product Code: 66701.
Staple Remover Kit. Terminated |
KDD | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.