Medical Device Manufacturer · US , Guntersville , AL

Kappler USA - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1996

Total

Cleared

Denied

Kappler USA has 2 FDA 510(k) cleared medical devices. Based in Guntersville, US.

Historical record: 2 cleared submissions from 1996 to 2000. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Kappler USA Filter by specialty or product code using the sidebar.

Kappler USA 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 - Kappler USA

2 devices

1-2 of 2