Medical Device Manufacturer · US , Mchenry , IL

Theratronics, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1982

Total

Cleared

Denied

Theratronics, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1982 to 1998. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Theratronics, Inc.

9 devices

1-9 of 9

THERAPLAN PLUS VERSION 1.2

THERAPLAN V05B/ TP-11 V09B

THERATRONIC STIMULATOR

K820782 · IPF

Physical Medicine · 72d

Theratronics, Inc. - FDA 510(k) Cleared Devices

Filters