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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stretcher, Hand-Carried
510(k) Number K900670
Device Name HARE EMERGENCY STRETCHER
Applicant
Dyna Corp.
6300 Yarrow Dr.
Carlsbad,  CA  92009
Applicant Contact R. A YAEGER
Correspondent
Dyna Corp.
6300 Yarrow Dr.
Carlsbad,  CA  92009
Correspondent Contact R. A YAEGER
Regulation Number880.6900
Classification Product Code
FPP  
Date Received02/13/1990
Decision Date 04/23/1990
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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