Invivo

FDA Filings

This page includes the latest FDA filings for Invivo. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Owner/Operator Registration

FDA Filings

Device Company	Device	Date
PMN K091902 INVIVO	1.5T 8-CHANNEL SMALL EXTREMITY COIL, MODEL 800494, 3.0T 8-CHANNEL SMALL EXTREMITY COIL, MODEL 800484	2009-08-21
PMN K082987 INVIVO	HRK-63-16 KNEE ARRAY COIL, HRK-127-16 KNEE ARRAY COIL	2008-11-06
PMN K082916 INVIVO	HRB-127-32 HIGH RESOLUTION BRAIN COIL	2008-10-15
PMN K072874 INVIVO	LBS-127-16 BREAST ARRAY COIL	2007-11-16
PMN K072873 INVIVO	LBS-63-16 BREAST ARRAY COIL	2007-11-16
PMN K061952 INVIVO	CARDIOVASCULAR ARRAY COILS, MODELS CAC-63-16, CAC-63-32, CAC-123-32 AND CAC-127-16	2006-07-28

Similar & Related FDA Registered Companies

• Invivoscribe, Inc.
• Invivo Corporation (Business Trade Name: Philips)
• Invivo Corporation
• INVIVO THERAPEUTICS CORPORATION
• INVIVO RESEARCH, INC.
• INVIVO RESEARCH LABS, INC.
• INVIVOSCRIBE TECHNOLOGIES, INC10222 Barnes Canyon Road, Building 1san Diego, CA 92121 PMA NumberP160040 Supplement NumberS010 Date Received03/15/2022 Decision Date04/11/2022 Product Code OWD  Advisory Committee Pathology Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
• INVIVOSCRIBE TECHNOLOGIES, INC