Theratronics, Inc.
Theratronics, Inc. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 4, 1998.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K983917 | THERATRON ELITE | December 4, 1998 |
| K970236 | THERAPLAN PLUS VERSION 1.2 | July 9, 1997 |
| K964606 | THERATRON 780E | June 26, 1997 |
| K964607 | THERATON 1000E | May 28, 1997 |
| K954679 | THERAPLAN PLUS | November 8, 1996 |
| K940237 | THERAPLAN V05B/ TP-11 V09B | July 26, 1994 |
| K922276 | THERAC 25 | May 25, 1994 |
| K894165 | THERATRON 1000 | February 1, 1990 |
| K820782 | THERATRONIC STIMULATOR | June 3, 1982 |