510(k) K961922 ยท HET Laparoscope, Gynecologic (And Accessories)
RDP-2
| Applicant | Ranfac, Corp., Avon MA, US |
| Decision | Substantially Equivalent, Aug 9, 1996 |
| Received | May 17, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961922
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.