510(k) K902830 ยท HED Douche Apparatus, Vaginal, Therapeutic
PERI-BOTTLE
| Applicant | Orion Life Systems, Inc., Wheeling IL, US |
| Decision | Substantially Equivalent, Aug 6, 1990 |
| Received | Jun 28, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902830
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.