VENTI-MONITOR MODEL 101— 510(k) K812041

Name: FDA 510(k) clearance K812041
Creator: U.S. Food and Drug Administration
Published: 1981-09-25

Substantially Equivalent

Medix Medical Electronics (U.S.A.), Inc.

FDA 510(k) clearance K812041 for VENTI-MONITOR MODEL 101, Substantially Equivalent on 1981-09-25. Applicant: Medix Medical Electronics (U.S.A.), Inc.. Device class: 2.

Clearance details

Applicant: Medix Medical Electronics (U.S.A.), Inc.
Product code: Code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 1981-07-21
Decision date: 1981-09-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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