Medical Device Manufacturer · US , Davenport , IA

Litton Systems, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1987

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Litton Systems, Inc. Radiology ✕

2 devices

1-2 of 2

Cleared Jun 19, 1995

PULSE KLYSTRON AMPLIFIFER (L-5822-90)

Radiology · 98d

Cleared Jun 16, 1995

PULSE KLYSTRON AMPLIFIER (L-5822-00)

Radiology · 95d