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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 K904494
Device Name HAND-CARRIED STRETCHERS
Applicant
Minto Research & Development, Inc.
3676 Charlanne Dr.
Redding,  CA  96002
Applicant Contact ROBERT WILLIAMS
Correspondent
Minto Research & Development, Inc.
3676 Charlanne Dr.
Redding,  CA  96002
Correspondent Contact ROBERT WILLIAMS
Regulation Number880.6900
Classification Product Code
FPP  
Date Received10/02/1990
Decision Date 10/12/1990
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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