510(k) K854493 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
ERG 555 COUCH ERGOMETER
| Applicant | Robert Bosch Corp., St. James NY, US |
| Decision | Substantially Equivalent, Jun 16, 1986 |
| Received | Nov 12, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854493
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.