510(k) K903724 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
BEAMER 1,2,4,6, AND 8
| Applicant | Beacon Laboratories, Inc., Broomfield CO, US |
| Decision | Substantially Equivalent, Sep 28, 1990 |
| Received | Aug 16, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903724
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.