The following data is part of a premarket notification filed by Hewlett-packard Gmbh with the FDA for Hp Viridia Component Monitoring System, Model Rev. K With Easi-st Segment Measurement, Hp Viridia Cms 24/26, Rev K With.
| Device ID | K992595 |
| 510k Number | K992595 |
| Device Name: | HP VIRIDIA COMPONENT MONITORING SYSTEM, MODEL REV. K WITH EASI-ST SEGMENT MEASUREMENT, HP VIRIDIA CMS 24/26, REV K WITH |
| Classification | Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) |
| Applicant | HEWLETT-PACKARD GMBH HERRENBERGER STR. 110-140 Boeblingen, DE 71034 |
| Contact | Egon Pfeil |
| Correspondent | Egon Pfeil HEWLETT-PACKARD GMBH HERRENBERGER STR. 110-140 Boeblingen, DE 71034 |
| Product Code | MHX |
| CFR Regulation Number | 870.1025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-08-03 |
| Decision Date | 1999-12-08 |
| Summary: | summary |