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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name catheters, suction, tracheobronchial
510(k) Number K870962
Device Name GESCO ASPIRATOR
Applicant
GESCO INTL., INC.
P.O. BOX 690188
SAN ANTONIO,  TX  78269
Applicant Contact GEORGE E SINKO
Correspondent
GESCO INTL., INC.
P.O. BOX 690188
SAN ANTONIO,  TX  78269
Correspondent Contact GEORGE E SINKO
Regulation Number868.6810
Classification Product Code
BSY  
Date Received03/10/1987
Decision Date 05/22/1987
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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