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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Fixation, Tracheal Tube
510(k) Number K902604
Device Name BLAKE MEDICAL BREATHING TUBE SUPPORT
Applicant
Blake Medical, Inc.
2803 Carmicheal Dr.
Tifton,  GA  31794
Applicant Contact MARK B LOTT
Correspondent
Blake Medical, Inc.
2803 Carmicheal Dr.
Tifton,  GA  31794
Correspondent Contact MARK B LOTT
Regulation Number868.5770
Classification Product Code
CBH  
Date Received06/12/1990
Decision Date 10/02/1990
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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