510(k) K933265 ยท MDM Instrument, Manual, Surgical, General Use
ACU-DISPO-CE(TM)
| Applicant | Acuderm, Inc., Ft. Lauderdale FL, US |
| Decision | Substantially Equivalent, Mar 7, 1994 |
| Received | Jul 6, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933265
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.