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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 K902474
Device Name WEEVAC 1 PORTABLE RESCUE STRETCHER
Applicant
W. Murphy Ent., Inc.
48 Southvale Dr., Toronto
Ontario,  CA M4G 1G3
Applicant Contact MURPHY R.T.
Correspondent
W. Murphy Ent., Inc.
48 Southvale Dr., Toronto
Ontario,  CA M4G 1G3
Correspondent Contact MURPHY R.T.
Regulation Number880.6900
Classification Product Code
FPP  
Date Received06/05/1990
Decision Date 07/24/1990
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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