REEVUE INDIRECT CALORIMETER, MODEL#8100— 510(k) K021490

Name: FDA 510(k) clearance K021490
Creator: U.S. Food and Drug Administration
Published: 2003-01-02

Substantially Equivalent

Korr Medical Technologies, Inc.

FDA 510(k) clearance K021490 for REEVUE INDIRECT CALORIMETER, MODEL#8100, Substantially Equivalent on 2003-01-02. Applicant: Korr Medical Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Korr Medical Technologies, Inc.
Product code: Code BZL
Device class: Class 2
Regulation: 21 CFR 868.1730
Advisory panel: Anesthesiology
Date received: 2002-05-09
Decision date: 2003-01-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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