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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
510(k) Number K905114
Device Name A.P.GRAPH III(TM) CARDIOVASCULAR ANALYZER
Applicant
Research Consultants, Inc.
135 Talmage Rd.
Mendham,  NJ  07945
Applicant Contact RAOUL DESJARDINS
Correspondent
Research Consultants, Inc.
135 Talmage Rd.
Mendham,  NJ  07945
Correspondent Contact RAOUL DESJARDINS
Regulation Number870.2780
Classification Product Code
JOM  
Date Received11/13/1990
Decision Date 05/07/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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