VITALOGRAPH - BREATHCO MONITOR— 510(k) K902113

Name: FDA 510(k) clearance K902113
Creator: U.S. Food and Drug Administration
Published: 1990-10-26

Substantially Equivalent

Mcneill Intl., Inc.

FDA 510(k) clearance K902113 for VITALOGRAPH - BREATHCO MONITOR, Substantially Equivalent on 1990-10-26. Applicant: Mcneill Intl., Inc.. Device class: 2.

Clearance details

Applicant: Mcneill Intl., Inc.
Product code: Code CCJ
Device class: Class 2
Regulation: 21 CFR 868.1430
Advisory panel: Anesthesiology
Date received: 1990-05-11
Decision date: 1990-10-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Willoughby, OH, US

Download summary PDF View on FDA.gov ↗

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