FDA 510(k) Applications Submitted by KEVIN CROSSEN

FDA 510(k) Number Submission Date Device Name Applicant
K120343 02/03/2012 CONNEX WORKSTATION WELCH ALLYN, INC.
K120743 03/12/2012 SPECULUM, VAGINAL, NONMETAL WELCH ALLYN, INC.
K120774 03/14/2012 ACUITY CENTRAL MONITORING STATION OR ACUITY CENTRAL MONITORING SYSTEM, MOBILE ACUITY LT, MOBILE ACUITY, MOBILE LT WELCH ALLYN, INC.
K121013 04/03/2012 CONNEX VITAL SIGNS MONITOR 6000 SERIES WELCH ALLYN, INC.
K121405 05/10/2012 PANOPTIC WELCH ALLYN, INC.
K131573 05/30/2013 CP150 ELECTROCARDIOGRAPH WELCH ALLYN, INC.
K141582 06/13/2014 CP150 ELECTROCARDIOGRAPH WITH SPIROMETRY OPTION WELCH ALLYN
K122058 07/13/2012 FLEXIPORT ECOCUFF WELCH ALLYN, INC.
K142356 08/25/2014 Connex Spot Monitor,901058 Vital Signs Monitor Core WELCH ALLYN, INC.
K132807 09/09/2013 MONITORING STATION, CONNEX(R) CENTRAL STATION (CS) WELCH ALLYN, INC.
K132808 09/11/2013 VITAL SIGNS MONITOR, CONNEX VITAL SIGNS MONITOR WELCH ALLYN, INC.
K112687 09/15/2011 CONNEX(R) VITAL SIGNS MONITOR 6000 SERIES WELCH ALLYN, INC.
K964987 12/13/1996 DATASCOPE PERCOR STAT - DL 9.5 FR. 25 AND 40CC INTRA-AORTIC BALLOON FOR OPTIONAL SHEATHLESS INSERTION AND PERCOR STAT -0 DATASCOPE CORP.


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