510(k) K142248 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Prostiva RF Therapy Generator, Prostiva RF Therapy Hand Piece, Prostiva RF Therapy Return Electrode, Prostiva RF Therapy Tubing System, Prostiva RF Therapy Telescope
| Applicant | Urologix, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Feb 20, 2015 |
| Received | Aug 14, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142248
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.