510(k) K933814 ยท GXY Electrode, Cutaneous
PHOTOSTRESS RECOVERY TESTER
| Applicant | Storz Instrument Co., St. Louis MO, US |
| Decision | Substantially Equivalent, Dec 8, 1993 |
| Received | Aug 4, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933814
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.