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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