510(k) K990125 ยท DSI Detector And Alarm, Arrhythmia
HP VIRIDIA COMPONENT MONITORING SYSTEM, MODEL REV. K
| Applicant | Hewlett-Packard GmbH, Boeblingen, DE |
| Decision | Substantially Equivalent, Jan 29, 1999 |
| Received | Jan 13, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K990125
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.