Philips Rtnet Radiotherapy Networking System
FDA 510(k)Class II (US FDA 510(k))
Identifiers
- 510(k) Number
- K924495 FDA 510(k)
- FDA Product Code
- IYE FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 892.5050 FDA 510(k)
- Regulation Number
- 892.5050 FDA 510(k)
- Advisory Committee
- Radiology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
The Philips Rtnet Radiotherapy Networking System is a medical device designed to support radiotherapy departments by providing a networking solution for data management and communication. It integrates with radiotherapy equipment to facilitate data transfer and coordinate treatment plans and patient data across various platforms.
This system is supplied by Philips Medical Systems, Inc. and has received FDA 510(k) clearance under the regulation number 892.5050.
Frequently asked questions
What is the purpose of the Philips Rtnet Radiotherapy Networking System?
This system is designed to support radiotherapy departments by providing a networking solution for data management and communication. It integrates with radiotherapy equipment to facilitate the transfer of data and coordinate patient treatment plans across various platforms.
What is the regulatory status of this system?
The Philips Rtnet Radiotherapy Networking System has received FDA 510(k) clearance under regulation number 892.5050. This indicates that the device has been reviewed and cleared for use by the FDA.
Who is the manufacturer of this networking system?
The system is supplied and manufactured by Philips Medical Systems, Inc., which is based in the Netherlands.
This description and any FAQs above were generated automatically from registry data and have not been verified by the manufacturer or by deviCERTS. Always check the official registry entry and the manufacturer's instructions for use before relying on them. Sources consulted: Philips RTnet Radiotherapy Networking System - Philips Medical Systems ..., PHILIPS RTNET RADIOTHERAPY NETWORKING SYSTEM (K924495) — FDA 510 (k ..., PDF K924495 - Philips Rtnet Radiotherapy Networking System, Global home | Philips
Authorization Coverage (1 country)
Regulatory Authorizations
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K924495 | Class II | Active |
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Manufacturer
- Manufacturer
- Philips Medical Systems, Inc.
Sources (1)
- FDA 510(k) K924495 24 fields · synced Sep 23, 2026