The following data is part of a premarket notification filed by Hewlett-packard Co. with the FDA for Hp M2600a Viridia Telemetry System.
| Device ID | K993516 |
| 510k Number | K993516 |
| Device Name: | HP M2600A VIRIDIA TELEMETRY SYSTEM |
| Classification | Detector And Alarm, Arrhythmia |
| Applicant | HEWLETT-PACKARD CO. 3000 MINUTEMAN ROAD, MS 0491 Andover, MA 01810 -1099 |
| Contact | Denise Haley |
| Correspondent | Denise Haley HEWLETT-PACKARD CO. 3000 MINUTEMAN ROAD, MS 0491 Andover, MA 01810 -1099 |
| Product Code | DSI |
| CFR Regulation Number | 870.1025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-10-18 |
| Decision Date | 1999-11-08 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00884838011359 | K993516 | 000 |
| 00884838011342 | K993516 | 000 |