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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name plethysmograph, pressure
510(k) Number K852102
Device Name COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEM
Applicant
WARREN E. COLLINS, INC.
220 WOOD RD.
BRAINTREE,  MA  02184 -2408
Applicant Contact JAMES TULLY
Correspondent
WARREN E. COLLINS, INC.
220 WOOD RD.
BRAINTREE,  MA  02184 -2408
Correspondent Contact JAMES TULLY
Regulation Number868.1750
Classification Product Code
CCM  
Date Received05/15/1985
Decision Date 07/31/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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