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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 K890425
Device Name NEOTECH MUCUS TRAP W/CATHETER
Applicant
Neotech Products, Inc.
9135 Alabama Ave., Suite F
Chatsworth,  CA  91311
Applicant Contact THOMAS R THORNBURY
Correspondent
Neotech Products, Inc.
9135 Alabama Ave., Suite F
Chatsworth,  CA  91311
Correspondent Contact THOMAS R THORNBURY
Regulation Number868.6810
Classification Product Code
BSY  
Date Received01/26/1989
Decision Date 04/19/1989
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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