SCANX D5000 SERIES SCANNER MODEL: D5000-F, D5000-FB, D5000-FVB, D5000-Q, D5000-QB— 510(k) K101289
Substantially EquivalentAir Techniques, Inc.
FDA 510(k) clearance K101289 for SCANX D5000 SERIES SCANNER MODEL: D5000-F, D5000-FB, D5000-FVB, D5000-Q, D5000-QB, Substantially Equivalent on 2010-08-03. Applicant: Air Techniques, Inc.. Device class: 2.
Clearance details
- Applicant
- Air Techniques, Inc.
- Product code
- Code MQB
- Device class
- Class 2
- Regulation
- 21 CFR 892.1680
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Melville, NY, US
Recent devices under product code MQB
view allMore clearances from Air Techniques, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.