510(k) K901553 ยท HLR Keratoscope, Battery-Powered
SURG-K SURGICAL KERATOMETER
| Applicant | The Sanborn Co., Santa Clara CA, US |
| Decision | Substantially Equivalent, Jul 20, 1990 |
| Received | Apr 3, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901553
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.