MONITOR, CITADEL INTRAVASCULAR PO2— 510(k) K760350

Name: FDA 510(k) clearance K760350
Creator: U.S. Food and Drug Administration
Published: 1976-10-29

Substantially Equivalent

Sherwood Medical Industries

FDA 510(k) clearance K760350 for MONITOR, CITADEL INTRAVASCULAR PO2, Substantially Equivalent on 1976-10-29. Applicant: Sherwood Medical Industries. Device class: 2.

Clearance details

Applicant: Sherwood Medical Industries
Product code: Code CCE
Device class: Class 2
Regulation: 21 CFR 868.1200
Advisory panel: Anesthesiology
Date received: 1976-08-02
Decision date: 1976-10-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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