510(k) K914381 ยท DRR Amplifier And Signal Conditioner, Biopotential
HORIZON 9000/HIS OPTION AMPLIFIER
| Applicant | Mennen Medical, Inc., Clarence NY, US |
| Decision | Substantially Equivalent, Jan 28, 1992 |
| Received | Oct 3, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914381
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.