510(k) K973193 ยท HQF Laser, Ophthalmic
LUXSCOPE
| Applicant | Luxtec Corp., Newton MA, US |
| Decision | Substantially Equivalent, Nov 21, 1997 |
| Received | Aug 25, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973193
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.