510(k) K991773 ยท DSI Detector And Alarm, Arrhythmia
HP VIRIDIA COMPONENT MONITORING SYSTEM, HP VIRIDIA CMS 24/26, HP VIRIDIA MULTI-MEASUREMENT SERVER AND COMPACT PORTABLE P
| Applicant | Hewlett-Packard GmbH, Boeblingen, DE |
| Decision | Substantially Equivalent, Jun 7, 1999 |
| Received | May 25, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K991773
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.