Panther TPS 6.0
Panther TPS 6.0 is a Class II device made by Prowess, Inc., listed in FDA GUDID since 19 Dec 2024 (UDI-DI 00859032007279), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00859032007279 | Date19 Dec 2024 | StatusListed |
Official records
- AccessGUDID record 00859032007279
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Panther TPS
- Generic name
- Radiation therapy software
- Model / reference
- 6.0
- Primary DI / UDI-DI
- 00859032007279
- 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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