510(k) K903744 ยท HIB Speculum, Vaginal, Nonmetal
PHYSICIAN'S CHOICE
| Applicant | Advance Medical Device, Inc., Ontario L3y 4v8, Canada, CA |
| Decision | Substantially Equivalent, Sep 12, 1990 |
| Received | Aug 16, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903744
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.