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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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