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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Sleeve, Limb, Compressible
510(k) Number K921608
Device Name PRESSSION, SEQUENTIAL
Applicant
Chattanooga Group, Inc.
4717 Adams Rd.
P.O. Box 4287
Hixson,  TN  37343
Applicant Contact GRAHAME R WATTS
Correspondent
Chattanooga Group, Inc.
4717 Adams Rd.
P.O. Box 4287
Hixson,  TN  37343
Correspondent Contact GRAHAME R WATTS
Regulation Number870.5800
Classification Product Code
JOW  
Date Received04/03/1992
Decision Date 12/30/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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