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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stretcher, Wheeled
510(k) Number K761147
Device Name RELIANCE MOD-U-LINE M-700
Applicant
F. & F. Koenigkramer
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
F. & F. Koenigkramer
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number880.6910
Classification Product Code
FPO  
Date Received11/26/1976
Decision Date 01/28/1977
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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