The following data is part of a premarket notification filed by Hewlett-packard Co. with the FDA for Hp Viridia Information System, Models M3150a/ M3151a/ M3153a/ M3154a.
| Device ID | K993171 |
| 510k Number | K993171 |
| Device Name: | HP VIRIDIA INFORMATION SYSTEM, MODELS M3150A/ M3151A/ M3153A/ M3154A |
| Classification | Detector And Alarm, Arrhythmia |
| Applicant | HEWLETT-PACKARD CO. 3000 MINUTEMAN RD. Andover, MA 01810 |
| Contact | Dave Osborn |
| Correspondent | Dave Osborn HEWLETT-PACKARD CO. 3000 MINUTEMAN RD. Andover, MA 01810 |
| Product Code | DSI |
| CFR Regulation Number | 870.1025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-09-21 |
| Decision Date | 1999-10-21 |
| Summary: | summary |