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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 K905381
Device Name MANHANDLER
Applicant
Lifeport, Inc.
12000 NE 95th St.
Suite 500
Vancouver,  WA  98682
Applicant Contact RANDY ROSANE
Correspondent
Lifeport, Inc.
12000 NE 95th St.
Suite 500
Vancouver,  WA  98682
Correspondent Contact RANDY ROSANE
Regulation Number880.6900
Classification Product Code
FPP  
Date Received11/29/1990
Decision Date 03/13/1991
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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