510(k) K911104 ยท FEX Instrument, Catheter, Punch
PHOTCOAGULATOR KR-568 LASER SPECTRUM ELITE K1
| Applicant | Hgm Medical Laser Systems, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jun 11, 1991 |
| Received | Mar 13, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911104
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.