510(k) K920187 ยท HHW Pessary, Vaginal
FLEXIBLE SILICONE GELIHORN
| Applicant | Bioteque America, Inc., Levittown PA, US |
| Decision | Substantially Equivalent, Oct 23, 1992 |
| Received | Jan 14, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920187
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.