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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Tube, Tracheal (W/Wo Connector)
510(k) Number K822082
Device Name SHERIDAN/HVT,CF, UNCUFFED
Applicant
Sheridan Catheter Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Sheridan Catheter Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number868.5730
Classification Product Code
BTR  
Date Received07/12/1982
Decision Date 08/10/1982
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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