The following data is part of a premarket notification filed by Hewlett-packard Co. with the FDA for Hp M2600a Viridia Telemetry System (formerly Known As The Hp 2600a Omni-care Telemetry System).
| Device ID | K980429 |
| 510k Number | K980429 |
| Device Name: | HP M2600A VIRIDIA TELEMETRY SYSTEM (FORMERLY KNOWN AS THE HP 2600A OMNI-CARE TELEMETRY SYSTEM) |
| Classification | Detector And Alarm, Arrhythmia |
| Applicant | HEWLETT-PACKARD CO. 3000 MINUTEMAN RD. Andover, MA 01810 -1085 |
| Contact | Ray Stelting |
| Correspondent | Ray Stelting HEWLETT-PACKARD CO. 3000 MINUTEMAN RD. Andover, MA 01810 -1085 |
| Product Code | DSI |
| CFR Regulation Number | 870.1025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-02-04 |
| Decision Date | 1998-09-09 |
| Summary: | summary |