510(k) K914241 ยท HHK Curette, Suction, Endometrial (And Accessories)
PIONEER PRO-PUMP DUAL CONTROL
| Applicant | Pioneer Medical, Inc., Branford CT, US |
| Decision | Substantially Equivalent, Mar 4, 1992 |
| Received | Sep 23, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914241
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.