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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Scale, Patient
510(k) Number K871771
Device Name COMFORTWEIGH
Applicant
Curlington Industrial Electronics, Inc.
Rte. 1, Box 433-D
Phenix City,  AL  36867
Applicant Contact G. R CURLINGTON
Correspondent
Curlington Industrial Electronics, Inc.
Rte. 1, Box 433-D
Phenix City,  AL  36867
Correspondent Contact G. R CURLINGTON
Regulation Number880.2720
Classification Product Code
FRW  
Date Received05/06/1987
Decision Date 06/24/1987
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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