Medical Device Manufacturer · US , Washington , DC

Kleinfeld, Kaplan and Becker - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1995

Total

Cleared

Denied

Kleinfeld, Kaplan and Becker has 2 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 2 cleared submissions from 1995 to 1996. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Kleinfeld, Kaplan and Becker Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Kleinfeld, Kaplan and Becker

2 devices

1-2 of 2