MODIFICATION TO AGILENT TECHNOLOGIES ANESTHESIA GAS MONITOR, MODEL M1026A #CO5— 510(k) K994188

Name: FDA 510(k) clearance K994188
Creator: U.S. Food and Drug Administration
Published: 2000-05-19

Substantially Equivalent

Agilent Technologies, GmbH

FDA 510(k) clearance K994188 for MODIFICATION TO AGILENT TECHNOLOGIES ANESTHESIA GAS MONITOR, MODEL M1026A #CO5, Substantially Equivalent on 2000-05-19. Applicant: Agilent Technologies, GmbH. Device class: 2.

Clearance details

Applicant: Agilent Technologies, GmbH
Product code: Code CBQ
Device class: Class 2
Regulation: 21 CFR 868.1500
Advisory panel: Anesthesiology
Date received: 1999-12-13
Decision date: 2000-05-19
Decision: Substantially Equivalent
Clearance type: Special
Location: Boeblingen, DE

Download summary PDF View on FDA.gov ↗

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