INTERFLO MEDICAL MODEL INTERFLO/1 CARDIAC OUTPUT— 510(k) K902628

Name: FDA 510(k) clearance K902628
Creator: U.S. Food and Drug Administration
Published: 1991-02-25

Substantially Equivalent

Biometric Research Institute, Inc.

FDA 510(k) clearance K902628 for INTERFLO MEDICAL MODEL INTERFLO/1 CARDIAC OUTPUT, Substantially Equivalent on 1991-02-25. Applicant: Biometric Research Institute, Inc.. Device class: 2.

Clearance details

Applicant: Biometric Research Institute, Inc.
Product code: Code DXG
Device class: Class 2
Regulation: 21 CFR 870.1435
Advisory panel: Cardiovascular
Date received: 1990-06-13
Decision date: 1991-02-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington, VA, US

Download summary PDF View on FDA.gov ↗

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