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FDA 510(k) Applications Submitted by INVIVO CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090785
03/23/2009
MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 865214
INVIVO CORP.
K051512
06/07/2005
CAC-127-8 CARDOAC ARRAY COIL
INVIVO CORP.
K052704
09/28/2005
MODEL BBD BREAST IMMOBILIZATION AND BIOPSY DEVICE
INVIVO CORP.
K052497
09/12/2005
NEUROVASCULAR ARRAY COIL, MODEL NVA-127-16-A
INVIVO CORP.
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