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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Ventilator, Continuous, Facility Use
510(k) Number K896269
Device Name SECHRIST VOLUME VENTILATOR MODEL 2200B
Applicant
Sechrist Industries, Inc.
2820 Gretta Ln.
Anaheim,  CA  92806
Applicant Contact SANDRA L DAVIS
Correspondent
Sechrist Industries, Inc.
2820 Gretta Ln.
Anaheim,  CA  92806
Correspondent Contact SANDRA L DAVIS
Regulation Number868.5895
Classification Product Code
CBK  
Date Received10/31/1989
Decision Date 05/18/1990
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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