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Panther TPS 5.7

by Prowess, Inc. 3 variants

Panther TPS 5.7 is a Class II device made by Prowess, Inc., listed in FDA GUDID since 1 Nov 2021 (UDI-DI 00859032007132), not in commercial distribution (GUDID) as of 9 Nov 2026.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00859032007132 UDI-DI Date1 Nov 2021ListedStatusListed GUDID: not in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Panther TPS
Generic name
Radiation therapy software
Model / reference
5.7
Primary DI / UDI-DI
00859032007132
FDA product code
MUJ
GMDN term
Radiation therapy software
Device class
Class II
Regulation number
892.5050
GUDID distribution status
Not in Commercial Distribution

Related devices

Category: Radiation therapy software

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Other devices filed under Radiation therapy software.

Other devices from Prowess, Inc.

See all devices from Prowess, Inc. →

Properties

  • Lot / batch number
  • Manufacturing date
Other properties (13, all answered No)