510(k) K913239 ยท HLZ Electrode, Corneal
GOLDLENS(TM)
| Applicant | Doran Instruments, Inc., Littleton MA, US |
| Decision | Substantially Equivalent, Jan 31, 1992 |
| Received | Jul 22, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913239
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.