510(k) K993907
- Device
- VIRIDIA INFORMATION CENTER SOFTWARE FOR M3154A OPT C22
- Applicant
- AGILENT TECHNOLOGIES, INC.
- 510(k) number
- K993907
- Product code
- MHD
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1999-12-06
- Date received
- 1999-11-17
- Regulation
- 880.5725
- Classification name
- Pump, Infusion, Gallstone Dissolution
- Medical specialty
- General Hospital
- Review panel
- General Hospital
- Device class
- 2
- Clearance type
- Special
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- DAVE OSBORN
- Address
- 3000 Minuteman Rd. Andover MA US 01810 01810
Source Documents#
Legacy Summary#
summary
FDA Review#
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