The following data is part of a premarket notification filed by Hewlett-packard Co. with the FDA for Hewlett-packard M1205a Viridia 24 Ct.
| Device ID | K981376 |
| 510k Number | K981376 |
| Device Name: | HEWLETT-PACKARD M1205A VIRIDIA 24 CT |
| Classification | Detector And Alarm, Arrhythmia |
| Applicant | HEWLETT-PACKARD CO. 3000 MINUTEMAN RD. Andover, MA 01810 -1085 |
| Contact | David Osborn |
| Correspondent | David Osborn 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 | 1998-04-16 |
| Decision Date | 1999-01-04 |
| Summary: | summary |