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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 K902503
Device Name HARE FOLDING BACK EMERGENCY STRETCHER
Applicant
Dyna Corp.
6300 Yarrow Dr.
Carlsbad,  CA  92009
Applicant Contact RICHARD A YAEGER
Correspondent
Dyna Corp.
6300 Yarrow Dr.
Carlsbad,  CA  92009
Correspondent Contact RICHARD A YAEGER
Regulation Number880.6910
Classification Product Code
FPO  
Date Received06/05/1990
Decision Date 06/26/1990
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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