510(k) K900630 ยท GEX Powered Laser Surgical Instrument
MODELS 4000/4900/6000/8000/8900, LUXAS&1700 ND:YAG
| Applicant | Heraeus Lasersonics, Inc., Milpitas CA, US |
| Decision | Substantially Equivalent, May 4, 1990 |
| Received | Feb 8, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900630
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.