510(k) K060752 ยท GEX Powered Laser Surgical Instrument
ACMI DUR-HL LASER SYSTEMS
| Applicant | Acmi Corporation, Southborough MA, US |
| Decision | Substantially Equivalent, May 25, 2006 |
| Received | Mar 21, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060752
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.