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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Airway, Esophageal (Obturator)
510(k) Number K864200
Device Name VETA/VENTED ESOPHAGEAL TUBE AIRWAY
Applicant
Cranco Co.
120 Oakwood Plz.
5320 S. 900 E.
Salt Lake City,  UT  84117
Applicant Contact RICHARD CRANGLE
Correspondent
Cranco Co.
120 Oakwood Plz.
5320 S. 900 E.
Salt Lake City,  UT  84117
Correspondent Contact RICHARD CRANGLE
Regulation Number868.5650
Classification Product Code
CAO  
Date Received10/27/1986
Decision Date 03/17/1987
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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