510(k) K920248 ยท GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered
MODEL SLASE 210 HOLMIUM LASER SYSTEM
| Applicant | Sunrise Technologies, Inc., Fremont CA, US |
| Decision | Unknown, Jul 21, 1992 |
| Received | Jan 21, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920248
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.