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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 K914607
Device Name SEHRIST VOLUME VENTILATOR, MODEL 2200B
Applicant
SECHRIST INDUSTRIES, INC.
4225 EAST LA PALMA
ANAHEIM,  CA  92807
Applicant Contact THOMAS R MEYERS
Correspondent
SECHRIST INDUSTRIES, INC.
4225 EAST LA PALMA
ANAHEIM,  CA  92807
Correspondent Contact THOMAS R MEYERS
Regulation Number868.5895
Classification Product Code
CBK  
Date Received10/17/1991
Decision Date 11/02/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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