510(k) K090281 ยท GEX Powered Laser Surgical Instrument
ACCUTECH FAMILY OF POWERFLEX LASER DELIVERY DEVICES
| Applicant | Accutech Medical Technologies, Inc., Pleasanton CA, US |
| Decision | Substantially Equivalent, Mar 4, 2009 |
| Received | Feb 5, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090281
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.