A.P.GRAPH III(TM) CARDIOVASCULAR ANALYZER— 510(k) K905114

Name: FDA 510(k) clearance K905114
Creator: U.S. Food and Drug Administration
Published: 1991-05-07

Substantially Equivalent

Research Consultants, Inc.

FDA 510(k) clearance K905114 for A.P.GRAPH III(TM) CARDIOVASCULAR ANALYZER, Substantially Equivalent on 1991-05-07. Applicant: Research Consultants, Inc.. Device class: 2.

Clearance details

Applicant: Research Consultants, Inc.
Product code: Code JOM
Device class: Class 2
Regulation: 21 CFR 870.2780
Advisory panel: Cardiovascular
Date received: 1990-11-13
Decision date: 1991-05-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mendham, NJ, US

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