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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 K932647
Device Name WIRE REINFORCED ENDOTRACHEAL TUBE
Applicant
VITAID, LTD.
269 PORTAGE RD.
LEWISTON,  NY  14092
Applicant Contact WILLIAM G STEWART
Correspondent
VITAID, LTD.
269 PORTAGE RD.
LEWISTON,  NY  14092
Correspondent Contact WILLIAM G STEWART
Regulation Number868.5730
Classification Product Code
BTR  
Date Received06/02/1993
Decision Date 11/02/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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