510(k) K944022 ยท HLM Instrument, Measuring, Lens, Ac-Powered
LENSCHEK
| Applicant | Leica, Inc., Buffalo NY, US |
| Decision | Substantially Equivalent, Nov 17, 1994 |
| Received | Aug 17, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944022
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.