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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name tube, aspirating, flexible, connecting
510(k) Number K790420
Device Name SUCTION CONNECTING TUBING
Applicant
SNYDER LABORATORIES, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
SNYDER LABORATORIES, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number880.6740
Classification Product Code
BYY  
Date Received02/28/1979
Decision Date 04/23/1979
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
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