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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Tube, Tracheostomy (W/Wo Connector)
510(k) Number K874742
Device Name QUICKTRACH
Applicant
Posey Co.
2443 Delta Ln.
Elk Grove Village,  IL  60007
Applicant Contact ERNEST M POSEY
Correspondent
Posey Co.
2443 Delta Ln.
Elk Grove Village,  IL  60007
Correspondent Contact ERNEST M POSEY
Regulation Number868.5800
Classification Product Code
BTO  
Date Received11/18/1987
Decision Date 12/31/1987
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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