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FDA 510(k)

KONICAMINOLTA DI-X1

K-Number: K212685 · 2021-09-13

ApplicantKonica Minolta, Inc.
Decision Date2021-09-13
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KONICAMINOLTA DI-X1 is a medical device manufactured by Konica Minolta, Inc.. It received FDA 510(k) clearance on 2021-09-13 under approval number K212685. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KONICAMINOLTA DI-X1?

KONICAMINOLTA DI-X1 is a medical device that received FDA 510(k) clearance on 2021-09-13. It is manufactured by Konica Minolta, Inc.. The 510(k) number is K212685.

When was KONICAMINOLTA DI-X1 approved by the FDA?

KONICAMINOLTA DI-X1 received FDA 510(k) clearance on 2021-09-13, under approval number K212685.

What company makes KONICAMINOLTA DI-X1?

KONICAMINOLTA DI-X1 is manufactured by Konica Minolta, Inc..

What is the FDA product code for KONICAMINOLTA DI-X1?

The FDA product code for KONICAMINOLTA DI-X1 is LLZ.

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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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