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FDA 510(k) Applications Submitted by JORDAN SCHRECK
FDA 510(k) Number
Submission Date
Device Name
Applicant
K051283
05/17/2005
MODIFICATION TO BERNOULLI VENTILATOR MANAGEMENT SYSTEM SOFTWARE
CARDIOPULMONARY CORP.
K091461
05/18/2009
BERNOULLI MANAGEMENT SYSTEM, OXINET III AND LIFEGARD VUE
CARDIOPULMONARY CORP.
K061932
07/07/2006
BERNOULLI MANAGEMENT SYSTEM (MS) SOFTWARE
CARDIOPULMONARY CORP.
K142043
07/28/2014
INSYNC ZR HIGH TRANSLUCENCY ZIRCONIA
JENSEN INDUSTRIES, INC.
K183408
12/10/2018
Jensen Shade Effect Liquids
Jensen Industries, Inc.
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