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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact