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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K945575
Device Name PRO BARRIER(TM) TUBE SOX(TM)
Applicant
Cottrell, Ltd.
49 Plain St.
North Attleboro,  MA  02760
Applicant Contact FRANK S CASCIANI
Correspondent
Cottrell, Ltd.
49 Plain St.
North Attleboro,  MA  02760
Correspondent Contact FRANK S CASCIANI
Classification Product Code
MMN
Date Received11/14/1994
Decision Date 03/06/1995
Decision Substantially Equivalent (SESE)
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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