REGIUS MODEL 170 DIRECT DIGITIZER— 510(k) K051998
Substantially EquivalentKonica Minolta Medical & Graphic, Inc.
FDA 510(k) clearance K051998 for REGIUS MODEL 170 DIRECT DIGITIZER, Substantially Equivalent on 2005-11-03. Applicant: Konica Minolta Medical & Graphic, Inc.. Device class: 2.
Clearance details
- Applicant
- Konica Minolta Medical & Graphic, 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
- Hachioji-Shi, JP
Recent devices under product code MQB
view allMore clearances from Konica Minolta Medical & Graphic, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.