AutoContour— 510(k) K200323
Substantially EquivalentRadformation, Inc.
FDA 510(k) clearance K200323 for AutoContour, Substantially Equivalent on 2020-10-30. Applicant: Radformation, Inc.. Device class: 2.
Clearance details
- Applicant
- Radformation, Inc.
- Product code
- Product code QKB
- Device class
- Class 2
- Regulation
- 21 CFR 892.2050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York, NY, US
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