Medical Device Manufacturer · US , Skillman , NJ

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

8 submissions · 8 cleared · Since 1984

Total

Cleared

Denied

Johnson & Johnson Consumer Products, Inc. has 8 FDA 510(k) cleared medical devices. Based in Skillman, US.

Historical record: 8 cleared submissions from 1984 to 2007. Primary specialty: General & Plastic Surgery.

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

Johnson & Johnson Consumer Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

8 devices

1-8 of 8