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FDA 510(k)

SKR 3000

K-Number: K223267 · 2022-11-17

ApplicantKonica Minolta, Inc.
Decision Date2022-11-17
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SKR 3000 is a medical device manufactured by Konica Minolta, Inc.. It received FDA 510(k) clearance on 2022-11-17 under approval number K223267. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SKR 3000?

SKR 3000 is a medical device that received FDA 510(k) clearance on 2022-11-17. It is manufactured by Konica Minolta, Inc.. The 510(k) number is K223267.

When was SKR 3000 approved by the FDA?

SKR 3000 received FDA 510(k) clearance on 2022-11-17, under approval number K223267.

What company makes SKR 3000?

SKR 3000 is manufactured by Konica Minolta, Inc..

What is the FDA product code for SKR 3000?

The FDA product code for SKR 3000 is MQB.

Other Devices by Konica Minolta, Inc.

K162065Ultrasound System SONIMAGE HS1 K162504SKR 3000 K172793SKR 3000 K171716SKR 3000 K182688SKR 3000 K182431Konicaminolta DI-X1

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Related Devices (Code: MQB)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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