510(k) K902000 ยท FZS Curette, Surgical, General Use
KEVTEK(TM) LASER DRAPE/ORGAN PROTECTOR/EYE SHIELD
| Applicant | Kevtek Medical Products, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Aug 21, 1990 |
| Received | May 2, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902000
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.