510(k) K920099 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
GYMMAN
| Applicant | Lumiscope Co., Inc., Edison NJ, US |
| Decision | Substantially Equivalent, Mar 9, 1992 |
| Received | Jan 9, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920099
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.