510(k) K010365 ยท MNG External Urethral Occluder, Urinary Incontinence-Control, Female
ORTHO CONTROL FEMALE URINARY CONTROL DEVICE
| Applicant | Personal Products Co., Skillman NJ, US |
| Decision | Substantially Equivalent, Apr 30, 2001 |
| Received | Feb 7, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010365
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.