The following data is part of a premarket notification filed by Hewlett-packard Gmbh with the FDA for Hp Viridia Component Monitoring System, Hp Viridia Cms 24/26, Hp Viridia Multi-measurement Server And Compact Portable T.
| Device ID | K990972 |
| 510k Number | K990972 |
| Device Name: | HP VIRIDIA COMPONENT MONITORING SYSTEM, HP VIRIDIA CMS 24/26, HP VIRIDIA MULTI-MEASUREMENT SERVER AND COMPACT PORTABLE T |
| Classification | Detector And Alarm, Arrhythmia |
| 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 | DSI |
| CFR Regulation Number | 870.1025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-03-23 |
| Decision Date | 1999-04-19 |
| Summary: | summary |