510(k) K973220 ยท HQF Laser, Ophthalmic
RODENSTOCK LASER SLITLAMP
| Applicant | G. Rodenstock Instrumente GmbH, Concord MA, US |
| Decision | Substantially Equivalent, Nov 4, 1997 |
| Received | Aug 27, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973220
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.