510(k) K011199 ยท HKY Tonometer, Manual
PROVIEW EYE PRESSURE MONITOR
| Applicant | Bausch & Lomb, Inc., Rochester NY, US |
| Decision | Substantially Equivalent, Jul 2, 2001 |
| Received | Apr 19, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011199
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.