VARIAN C/D-SERIES CLINACS (CLINAC 600 C/D)— 510(k) K926321

Substantially Equivalent

Varian Assoc., Inc.

FDA 510(k) clearance K926321 for VARIAN C/D-SERIES CLINACS (CLINAC 600 C/D), Substantially Equivalent on 1994-08-09. Applicant: Varian Assoc., Inc..

Clearance details

Applicant: Varian Assoc., Inc.
Product code: Code IYE
Advisory panel: Radiology
Date received: 1992-12-16
Decision date: 1994-08-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palo Alto, CA, US

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Adverse events under product code IYE

product code IYE

Malfunction: 455
Other: 3
Total: 458

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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