510(k) K870773 ยท LLF Laser, Neurosurgical, Argon
ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASER
| Applicant | Hgm, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jul 10, 1987 |
| Received | Feb 26, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870773
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.