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FDA 510(k) Applications Submitted by Jessica Stenberg
FDA 510(k) Number
Submission Date
Device Name
Applicant
K130499
02/26/2013
IU22 DIAGNOSTIC ULTRASOUND SYSTEM
PHILIPS ULTRASOUND, INC.
K172162
07/18/2017
ACUSON S3000 S2000 S1000 Diagnostic Ultrasound Systems
Siemens Healthcare
K132304
07/24/2013
EPIQ DIAGNOSTIC ULTRASOUND SYSTEM
PHILIPS ULTRASOUND, INC.
K110645
03/04/2011
BIO Z CARDIO PROFILE HEMODYNAMIC MONITOR
SONOSITE,INC.
K102390
08/23/2010
SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM
SONOSITE,INC.
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