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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 K760504
Device Name PLETHYSMOGRAPH (MDI SYSTEM II)
Applicant
Marketing Development Intl.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Marketing Development Intl.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number870.2780
Classification Product Code
JOM  
Date Received08/23/1976
Decision Date 08/26/1976
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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