Medical Device Manufacturer · US , Fort Washington , PA

Johnson & Johnson Consumer, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2018

Total

Cleared

Denied

Johnson & Johnson Consumer, Inc. has 2 FDA 510(k) cleared medical devices. Based in Fort Washington, US.

Historical record: 2 cleared submissions from 2018 to 2018. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Johnson & Johnson Consumer, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Johnson & Johnson Consumer, Inc.

2 devices

1-2 of 2