510(k) K993122 ยท HNO Keratome, Ac-Powered
MSP M/K BLADE
| Applicant | Medical Sterile Products, Inc., Rincon PR, US |
| Decision | Substantially Equivalent, Mar 16, 2000 |
| Received | Sep 20, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993122
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.