Medical Device Manufacturer · US , Wood Dale , IL

Pro-Tronics, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1989

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Pro-Tronics, Inc. Radiology ✕

5 devices

1-5 of 5

Cleared Apr 11, 1995

MOBIL C-ARM, REGURBISHED, VARIOUS MODELS

Radiology · 49d

Cleared Mar 14, 1995

GENERAL ELECTRIC AMX 110, AMX II AND AMX 3

Radiology · 183d

Cleared Jul 02, 1990

GENERAL ELECTRIC AMX 3

Radiology · 20d

Cleared May 03, 1989

GENERAL ELECTRIC AMX 110

Radiology · 61d

Cleared May 01, 1989

GENERAL ELECTRIC AMX II

Radiology · 59d

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: Apr 27, 2026