FDA 510(k) Applications Submitted by INVIVO

FDA 510(k) Number Submission Date Device Name Applicant
K082987 10/07/2008 HRK-63-16 KNEE ARRAY COIL, HRK-127-16 KNEE ARRAY COIL INVIVO
K091902 06/25/2009 1.5T 8-CHANNEL SMALL EXTREMITY COIL, MODEL 800494, 3.0T 8-CHANNEL SMALL EXTREMITY COIL, MODEL 800484 INVIVO
K082916 09/30/2008 HRB-127-32 HIGH RESOLUTION BRAIN COIL INVIVO
K072873 10/09/2007 LBS-63-16 BREAST ARRAY COIL INVIVO
K072874 10/09/2007 LBS-127-16 BREAST ARRAY COIL INVIVO
K061952 07/10/2006 CARDIOVASCULAR ARRAY COILS, MODELS CAC-63-16, CAC-63-32, CAC-123-32 AND CAC-127-16 INVIVO


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