510(k) K864065 ยท HNO Keratome, Ac-Powered
BKS-42 DISPOSABLE VACUUM TUBING PACK
| Applicant | Allergan, Inc., Santa Ana CA, US |
| Decision | Substantially Equivalent, Dec 15, 1986 |
| Received | Oct 20, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864065
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.