XIMAVIEW(TM)— 510(k) K884323

Substantially Equivalent

Varian Assoc., Inc.

FDA 510(k) clearance K884323 for XIMAVIEW(TM), Substantially Equivalent on 1989-04-03. Applicant: Varian Assoc., Inc.. Device class: 2.

Clearance details

Applicant: Varian Assoc., Inc.
Product code: Code KPQ
Device class: Class 2
Regulation: 21 CFR 892.5840
Advisory panel: Radiology
Date received: 1988-10-14
Decision date: 1989-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palo Alto, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.