510(k) K935301 ยท HGM System, Monitoring, Perinatal
R & D BATTERIES, INC. PART NUMBERS 5235, 5506 & 5050
| Applicant | R & D Batteries, Inc., Burnsville MN, US |
| Decision | Substantially Equivalent, Dec 5, 1994 |
| Received | Nov 3, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935301
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.