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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Bed, Manual
510(k) Number K885241
Device Name BED, ADJUSTABLE, HOSPITAL, FOLDING, FIELD, W/O MAT
Applicant
King Mfg. Co.
2605 Summer Ave.
P.O. Box 3064
Memphis,  TN  38112
Applicant Contact LAWRENCE E BRIGHT
Correspondent
King Mfg. Co.
2605 Summer Ave.
P.O. Box 3064
Memphis,  TN  38112
Correspondent Contact LAWRENCE E BRIGHT
Regulation Number880.5120
Classification Product Code
FNJ  
Date Received12/21/1988
Decision Date 02/24/1989
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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