510(k) K011708 ยท GEH Unit, Cryosurgical, Accessories
MODIFICATION TO WARTNER WART REMOVAL SYSTEM
| Applicant | Wartner Medical Products, Brampton, Ontario, CA |
| Decision | Substantially Equivalent, Feb 20, 2002 |
| Received | Jun 4, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011708
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.