510(k) K935634 ยท HGI Electrocautery, Gynecologic (And Accessories)
WALLACH LEEP PROCEDURE KIT
| Applicant | Wallach Surgical Devices, Inc., Milford CT, US |
| Decision | Substantially Equivalent, Jul 20, 1994 |
| Received | Nov 23, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935634
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.