510(k) K880734 ยท HHI System, Abortion, Vacuum
SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS
| Applicant | Personal Products Co., Milltown NJ, US |
| Decision | Substantially Equivalent, Apr 25, 1988 |
| Received | Feb 24, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880734
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.