510(k) K120431 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
HALO90 ULTRA ABLATION CATHETER
| Applicant | Barrx Medical, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, May 3, 2012 |
| Received | Feb 13, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120431
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.