SKR 3000— 510(k) K250665
Substantially EquivalentKonica Minolta, Inc.
FDA 510(k) clearance K250665 for SKR 3000, Substantially Equivalent on 2025-06-17. 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
- Tokyo, JP
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