FDA 510(k) Applications Submitted by JESSICA R 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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