510(k) K042211 ยท GEX Powered Laser Surgical Instrument
MODIFICATION TO: LASERPRO 810, 940, AND 980 DIODE DIODE LASER SYSTEMS
| Applicant | Surgical Laser Technologies, Inc., Montgomeryville PA, US |
| Decision | Substantially Equivalent, Nov 8, 2004 |
| Received | Aug 16, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042211
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.