510(k) K992595 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
HP VIRIDIA COMPONENT MONITORING SYSTEM, MODEL REV. K WITH EASI-ST SEGMENT MEASUREMENT, HP VIRIDIA CMS 24/26, REV K WITH
| Applicant | Hewlett-Packard GmbH, Boeblingen, DE |
| Decision | Substantially Equivalent, Dec 8, 1999 |
| Received | Aug 3, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K992595
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.