DIRECT DIGITIZER, REGIUS MODEL 210— 510(k) K092717
Substantially EquivalentKonica Minolta Medical & Graphic, Inc.
FDA 510(k) clearance K092717 for DIRECT DIGITIZER, REGIUS MODEL 210, Substantially Equivalent on 2009-10-30. 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
- Special
- Location
- New York, NY, US
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