AIMI-Triage CXR PTX— 510(k) K193300
Substantially EquivalentRadlogics, Inc.
FDA 510(k) clearance K193300 for AIMI-Triage CXR PTX, Substantially Equivalent on 2020-04-08. Applicant: Radlogics, Inc.. Device class: 2.
Clearance details
- Applicant
- Radlogics, Inc.
- Product code
- Code QFM
- Device class
- Class 2
- Regulation
- 21 CFR 892.2080
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Boston, MA, US
Recent devices under product code QFM
view allMore clearances from Radlogics, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.