K242957
- 510(k) number
- K242957
- Device name
- Identify (4.0)
- Applicant
- Varian Medical Systems, Inc. CA · US
- Product code
- IYE — Accelerator, Linear, Medical
- Decision date
- 2025-02-07
- Date received
- 2024-09-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.4 MB · U.S. public domain
Also available from FDA: K242957.pdf
Official FDA record: K242957
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.