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..
Clearance details
- Applicant
- Konica Minolta Technoproduct Co., Ltd.
- Product code
- Code MQB
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.