Medical Device Manufacturer · US , Raynham , MA

Johnson & Johnson - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2011

Recent clearances: SPOTLIGHT ACCESS SYSTEM, SPOTLIGHT ACCESS SYSTEM, COUGAR SYSTEM

View 9 510(k) Devices ↓ Official Website

9

Total

9

Cleared

0

Denied

FDA 510(k) Regulatory Record - Johnson & Johnson Neurology ✕

2 devices

1-2 of 2

Cleared Jan 27, 2012

SPOTLIGHT ACCESS SYSTEM

Neurology · 81d

Cleared Dec 16, 2011

SPOTLIGHT ACCESS SYSTEM

Neurology · 74d