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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 K924275
Device Name RESTRAINING STRETCHER
Applicant
Dms
600 S. Kiwanis
Soiux Falls,  SD  57104
Applicant Contact GILBER HOOGENDOORM
Correspondent
Dms
600 S. Kiwanis
Soiux Falls,  SD  57104
Correspondent Contact GILBER HOOGENDOORM
Regulation Number880.6900
Classification Product Code
FPP  
Date Received08/25/1992
Decision Date 07/27/1993
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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