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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stretcher, Wheeled
510(k) Number K873181
Device Name STRETCHER, WHEELED, MECHANICAL
Applicant
Cambridge Technologies, Inc.
300 Muir St.
Cambridge,  MD  21613
Applicant Contact DONALD HOLDT
Correspondent
Cambridge Technologies, Inc.
300 Muir St.
Cambridge,  MD  21613
Correspondent Contact DONALD HOLDT
Regulation Number880.6910
Classification Product Code
FPO  
Date Received08/12/1987
Decision Date 10/09/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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