510(k) K020482 ยท HNO Keratome, Ac-Powered
KERATOME BLADE 200200 & 600600
| Applicant | Micro Specialties, Inc., Milford CT, US |
| Decision | Substantially Equivalent, Dec 16, 2002 |
| Received | Feb 13, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020482
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.