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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K850740
Device Name SECHRIST VOLUME VENTILATOR MODIFICATION
Applicant
Sechrist Industries, Inc.
2820 Gretta Ln.
Anaheim,  CA  92806
Applicant Contact EDWIN WENINGER
Correspondent
Sechrist Industries, Inc.
2820 Gretta Ln.
Anaheim,  CA  92806
Correspondent Contact EDWIN WENINGER
Date Received01/28/1985
Decision Date 07/29/1985
Decision Substantially Equivalent (SESE)
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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