ELECTROMAGNETIC BLOOD & ARTERIAL GAUGE— 510(k) K801802

Name: FDA 510(k) clearance K801802
Creator: U.S. Food and Drug Administration
Published: 1981-01-02

Substantially Equivalent

Medical Testing System, Inc.

FDA 510(k) clearance K801802 for ELECTROMAGNETIC BLOOD & ARTERIAL GAUGE, Substantially Equivalent on 1981-01-02. Applicant: Medical Testing System, Inc.. Device class: 2.

Clearance details

Applicant: Medical Testing System, Inc.
Product code: Code DPW
Device class: Class 2
Regulation: 21 CFR 870.2100
Advisory panel: Cardiovascular
Date received: 1980-07-29
Decision date: 1981-01-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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