510(k) K081774 ยท HQF Laser, Ophthalmic
SOLX 790 TITANIUM SAPPHIRE LASER
| Applicant | Solx, Inc., Waltham MA, US |
| Decision | Substantially Equivalent, Sep 12, 2008 |
| Received | Jun 23, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081774
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.