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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Connector, Airway (Extension)
510(k) Number K850964
Device Name DOUBLE-SWIVEL CONNECTOR
Applicant
Sheridan Catheter Corp.
Route 40
Argyle,  NY  12809
Applicant Contact JOHN A STEEN
Correspondent
Sheridan Catheter Corp.
Route 40
Argyle,  NY  12809
Correspondent Contact JOHN A STEEN
Regulation Number868.5810
Classification Product Code
BZA  
Date Received03/08/1985
Decision Date 05/14/1985
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
Recalls CDRH Recalls
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