510(k) K962354 ยท GEX Powered Laser Surgical Instrument
DIOMED 15, 30, 60 SURGICAL DIODE LASER
| Applicant | Lifestream Int'L, Inc., North Attleboro MA, US |
| Decision | Substantially Equivalent, Sep 11, 1996 |
| Received | Jun 18, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962354
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.