|
Device Name
|
Applicant
|
510(K) Number
|
Decision Date
|
iu22 ultrasound system and transducers
|
PHILIPS ULTRASOUND, INC.
|
K093563 |
02/01/2010
|
cx50 diagnostic ultrasound system
|
PHILIPS ULTRASOUND, INC.
|
K111513 |
06/24/2011
|
cx50 3.0 diagnostic ultrasound system
|
PHILIPS ULTRASOUND, INC.
|
K123754 |
12/21/2012
|
iu22 diagnostic ultrasound system
|
PHILIPS ULTRASOUND, INC.
|
K130499 |
06/18/2013
|
epiq diagnostic ultrasound system
|
PHILIPS ULTRASOUND, INC.
|
K132304 |
08/21/2013
|
nuvis diagnostic ultrasound system
|
PHILIPS ULTRASOUND, INC.
|
K133833 |
01/17/2014
|
visiq diagnostic ultra sound system
|
PHILIPS ULTRASOUND, INC.
|
K141369 |
07/02/2014
|
epiq 5 diagnostic ultrasound system, epiq 7diagnostic ultrasound system, affiniti 50 diagnostic ultrasound system, affiniti 70 diagnostic ultrasound system
|
PHILIPS ULTRASOUND, INC.
|
K160807 |
04/06/2016
|
epiq 5 diagnostic ultrasound system; epiq 7 diagnostic ultrasound system; affiniti 50 diagnostic ultrasound system; affiniti 70 diagnostic ultrasound system
|
Philips Ultrasound, Inc.
|
K163120 |
01/10/2017
|
epiq , epiq 5, epiq 7, affiniti 30, affiniti 50 and affiniti 70 diagnostic ultrasound system
|
Philips Ultrasound, Inc.
|
K181485 |
07/27/2018
|
|