VIRIDIA INFORMATION CENTER SOFTWARE FOR M3154A OPT C22— 510(k) K993907

Name: FDA 510(k) clearance K993907
Creator: U.S. Food and Drug Administration
Published: 1999-12-06

Substantially Equivalent

Agilent Technologies, Inc.

FDA 510(k) clearance K993907 for VIRIDIA INFORMATION CENTER SOFTWARE FOR M3154A OPT C22, Substantially Equivalent on 1999-12-06. Applicant: Agilent Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Agilent Technologies, Inc.
Product code: Code MHD
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1999-11-17
Decision date: 1999-12-06
Decision: Substantially Equivalent
Clearance type: Special
Location: Andover, MA, US

Download summary PDF View on FDA.gov ↗

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