510(k) K080200 ยท HED Douche Apparatus, Vaginal, Therapeutic
WATER WORKS DOUCHING DEVICE
| Applicant | Abbott Research Group, Inc., North Attleboro MA, US |
| Decision | Substantially Equivalent, Jul 10, 2008 |
| Received | Jan 25, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080200
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.