510(k) K903912 ยท HNO Keratome, Ac-Powered
KERATOME
| Applicant | Micro Precision Instrument Co., Scottsdale AR, US |
| Decision | Substantially Equivalent, Oct 17, 1990 |
| Received | Aug 24, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903912
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.