CADPLAN BT— 510(k) K954467

Substantially Equivalent

Varian Assoc., Inc.

FDA 510(k) clearance K954467 for CADPLAN BT, Substantially Equivalent on 1996-03-15. Applicant: Varian Assoc., Inc.. Device class: 2.

Clearance details

Applicant: Varian Assoc., Inc.
Product code: Code JAQ
Device class: Class 2
Regulation: 21 CFR 892.5700
Advisory panel: Radiology
Date received: 1995-09-26
Decision date: 1996-03-15
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.