Eclipse Treatment Planning System 13.7
by Varian Medical Systems, Inc.
Eclipse Treatment Planning System 13.7 is a Class II device made by Varian Medical Systems, Inc., cleared under FDA 510(k) K152393 on 18 Sep 2015 and listed in FDA GUDID since 16 Sep 2016 (UDI-DI 00855141006004), active as of 8 Nov 2026. One FDA recall is linked to it.
Active
510(k)
Valid until
No expiry
FDA recalls
None ongoingDocuments
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00855141006004 | Date16 Sep 2016 | StatusListed |
| United States | FDA 510(k) | NumberK152393 | Date18 Sep 2015 | StatusActive |
Official records
- AccessGUDID record 00855141006004
- FDA 510(k) database K152393
Across registries
- FDA 510(k) K152393 decided 18 Sep 2015 Active
- FDA GUDID UDI-DI 00855141006004 listed 16 Sep 2016 Listed
Recalls
-
- Terminated Z-0805-2016
When using PBC 11.0.31 to calculate the dose for a conventional arc field with more than 100 segments for Eclipse versions 11.0, 13.0, 13.5 or 13.6, the displayed dose does not correspond to the calculated Monitor Units (MU). Potential for unintended radiation exposure.
Timeline
- Cleared FDA 510(k) K152393
- Recall initiated FDA recalls Z-0805-2016
- Listed FDA GUDID 00855141006004
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Eclipse Treatment Planning System
- Generic name
- Radiation therapy software
- Model / reference
- 13.7
- Primary DI / UDI-DI
- 00855141006004
- 510(k) Number
- FDA product code
- MUJ
- GMDN term
- Radiation therapy software
- Device class
- Class II
- Regulation number
- 892.5050
- GUDID distribution status
- In Commercial Distribution
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