510(k) K870807 ยท HNO Keratome, Ac-Powered
BKS-1000 REFRACTIVE SET USE IN KERATOREFRACTIVE
| Applicant | Allergan, Inc., Santa Ana CA, US |
| Decision | Substantially Equivalent, May 29, 1987 |
| Received | Feb 27, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870807
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.