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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name chamber, hyperbaric
510(k) Number K950386
Device Name MODEL 3200P/3200PR HYPERBARIC CHAMBER
Applicant
SECHRIST INDUSTRIES, INC.
4225 EAST LA PALMA
ANAHEIM,  CA  92807
Applicant Contact KAORU LEE ADAIR
Correspondent
SECHRIST INDUSTRIES, INC.
4225 EAST LA PALMA
ANAHEIM,  CA  92807
Correspondent Contact KAORU LEE ADAIR
Regulation Number868.5470
Classification Product Code
CBF  
Date Received02/01/1995
Decision Date 06/13/1995
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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