510(k) K940647 ยท HLQ Keratoscope, Ac-Powered
ORBSCAN(TM) KERATOMETER
| Applicant | Orbtek, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jul 6, 1994 |
| Received | Feb 15, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940647
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.