510(k) K844409 ยท HLZ Electrode, Corneal
DTL ELECTRODE
| Applicant | Sauquoit Industries, Inc., Scranton PA, US |
| Decision | Substantially Equivalent, Feb 14, 1985 |
| Received | Nov 14, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844409
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.