510(k) K920633 ยท KXP Stent, Vaginal
PESSARY FLEXIBLE SILICONE NICHOLS
| Applicant | Bioteque America, Inc., Langhorne PA, US |
| Decision | Substantially Equivalent, Nov 8, 1995 |
| Received | Feb 12, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920633
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.