The following data is part of a premarket notification filed by Hewlett-packard Co. with the FDA for Hewlett-packard Centralvue Software.
| Device ID | K964832 |
| 510k Number | K964832 |
| Device Name: | HEWLETT-PACKARD CENTRALVUE SOFTWARE |
| 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 | 1996-12-02 |
| Decision Date | 1997-05-15 |
| Summary: | summary |