SKR 3000— 510(k) K210619
Substantially EquivalentKonica Minolta, Inc.
FDA 510(k) clearance K210619 for SKR 3000, Substantially Equivalent on 2021-08-24. Applicant: Konica Minolta, Inc.. Device class: 2.
Clearance details
- Applicant
- Konica Minolta, 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
- Hino-Shi, JP
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