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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stimulator, Nerve, Battery-Powered
510(k) Number K954525
Device Name SENSI-TOUCH EPIDURAL ANESTHESIA FILTER
Applicant
Sherwood Medical Co.
1831 Olive St.
St. Louis,  MS  63103
Applicant Contact DENNIS POZZO
Correspondent
Sherwood Medical Co.
1831 Olive St.
St. Louis,  MS  63103
Correspondent Contact DENNIS POZZO
Regulation Number868.2775
Classification Product Code
BXN  
Date Received09/29/1995
Decision Date 01/19/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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