Intracavitary/Interstitial System— 510(k) K250289

Substantially Equivalent

Varian Medical Systems

FDA 510(k) clearance K250289 for Intracavitary/Interstitial System, Substantially Equivalent on 2025-04-25. Applicant: Varian Medical Systems. Device class: 2.

Clearance details

Applicant
Varian Medical Systems
Product code
Code JAQ
Device class
Class 2
Regulation
21 CFR 892.5700
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Palo Alto, CA, US
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