510(k) K101592 ยท GXD Generator, Lesion, Radiofrequency
ERASE HAND- HELD CONTROLLER; ERASE SINGLE USE ELECTRIC CATRIDGE SYSTEM
| Applicant | Cheng Medical, Corporation, Saratoga CA, US |
| Decision | Substantially Equivalent, Oct 6, 2011 |
| Received | Jun 7, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101592
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.