Medical Device Manufacturer · US , Florida , FL

Invivo - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2006

6

Total

6

Cleared

0

Denied

Invivo has 6 FDA 510(k) cleared medical devices. Based in Florida, US.

Historical record: 6 cleared submissions from 2006 to 2009. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Invivo Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Invivo

6 devices

1-6 of 6

Cleared Aug 21, 2009

1.5T 8-CHANNEL SMALL EXTREMITY COIL, MODEL 800494, 3.0T 8-CHANNEL SMALL...

Radiology · 57d

Cleared Nov 06, 2008

HRK-63-16 KNEE ARRAY COIL, HRK-127-16 KNEE ARRAY COIL

Radiology · 30d

Cleared Oct 15, 2008

HRB-127-32 HIGH RESOLUTION BRAIN COIL

Radiology · 15d

Cleared Nov 16, 2007

LBS-63-16 BREAST ARRAY COIL

Radiology · 38d

Cleared Nov 16, 2007

LBS-127-16 BREAST ARRAY COIL

Radiology · 38d

Cleared Jul 28, 2006

CARDIOVASCULAR ARRAY COILS, MODELS CAC-63-16, CAC-63-32, CAC-123-32 AND...

Radiology · 18d