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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 K920805
Device Name LIFE LITE EMERGENCY STRETCHER
Applicant
Design Principles, Inc.
190 Lime Quarry Rd.
Suite 106
Madison,  AL  35758
Applicant Contact THOMAS M DEMPSEY
Correspondent
Design Principles, Inc.
190 Lime Quarry Rd.
Suite 106
Madison,  AL  35758
Correspondent Contact THOMAS M DEMPSEY
Regulation Number880.6900
Classification Product Code
FPP  
Date Received02/21/1992
Decision Date 05/22/1992
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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