The following data is part of a premarket notification filed by Agilent Technologies, Inc. with the FDA for Viridia Information Center Software For M3154a Opt C22.
| Device ID | K993907 |
| 510k Number | K993907 |
| Device Name: | VIRIDIA INFORMATION CENTER SOFTWARE FOR M3154A OPT C22 |
| Classification | Pump, Infusion, Gallstone Dissolution |
| Applicant | AGILENT TECHNOLOGIES, INC. 3000 MINUTEMAN RD. Andover, MA 01810 -1099 |
| Contact | Dave Osborn |
| Correspondent | Dave Osborn AGILENT TECHNOLOGIES, INC. 3000 MINUTEMAN RD. Andover, MA 01810 -1099 |
| Product Code | MHD |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-11-17 |
| Decision Date | 1999-12-06 |
| Summary: | summary |