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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Support, Patient Position
510(k) Number K943837
Device Name CHIN UP
Applicant
Edward Carden
4 Jib St. #14
Marina Del Rey,  CA  90292
Applicant Contact EDWARD HARDY
Correspondent
Edward Carden
4 Jib St. #14
Marina Del Rey,  CA  90292
Correspondent Contact EDWARD HARDY
Regulation Number868.6820
Classification Product Code
CCX  
Date Received08/05/1994
Decision Date 10/14/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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