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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K862434
Device Name SUCTION T CONNECTOR
Applicant
Acutronic Medical Systems AG
Kreuzstrasse 100
Jona-Rapper Swril,  CH 8645
Applicant Contact AJAI P SINGH
Correspondent
Acutronic Medical Systems AG
Kreuzstrasse 100
Jona-Rapper Swril,  CH 8645
Correspondent Contact AJAI P SINGH
Date Received06/26/1986
Decision Date 07/10/1986
Decision Substantially Equivalent (SESE)
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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