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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