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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Set, Tubing And Support, Ventilator (W Harness)
510(k) Number K770593
Device Name CORRUGATED TUBING #770 & 771
Applicant
Surgicot, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Surgicot, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number868.5975
Classification Product Code
BZO  
Date Received03/28/1977
Decision Date 04/19/1977
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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