DIGITAL RADIOGRAPHY, FLEXDR C30— 510(k) K082347
Substantially EquivalentKonica Minolta Technoproduct Co., Ltd.
FDA 510(k) clearance K082347 for DIGITAL RADIOGRAPHY, FLEXDR C30, Substantially Equivalent on 2008-11-18. Applicant: Konica Minolta Technoproduct Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Konica Minolta Technoproduct Co., Ltd.
- 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
- New York, NY, US
Recent devices under product code MQB
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