Panther OIS|R&V

GUDID 00859032007033

Panther OIS|R&V 2.2 DCP

Prowess, Inc.

Radiation therapy treatment record/verify system

• Primary Device ID: 00859032007033
• NIH Device Record Key: 8ada6fe7-9e37-41d1-bb33-fd6655f3ab8e
• Commercial Distribution Discontinuation: 2024-12-19
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Panther OIS|R&V
• Version Model Number: 2.2
• Company DUNS: 002162728
• Company Name: Prowess, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00859032007033 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K211760

FDA Product Code

• IYE: Accelerator, Linear, Medical

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-12-27
• Device Publish Date: 2024-12-19

On-Brand Devices [Panther OIS|R&V]

• 00859032007095: v2.31
• 00859032007033: Panther OIS|R&V 2.2 DCP