CTM (CLINAC TREATMENT MONITOR)— 510(k) K770202

Name: FDA 510(k) clearance K770202
Creator: U.S. Food and Drug Administration
Published: 1977-02-07

Substantially Equivalent

Varian Assoc., Inc.

FDA 510(k) clearance K770202 for CTM (CLINAC TREATMENT MONITOR), Substantially Equivalent on 1977-02-07. 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: 1977-01-31
Decision date: 1977-02-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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