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FDA 510(k)

Konicaminolta DI-X1

K-Number: K230906 · 2023-04-25

ApplicantKonica Minolta, Inc.
Decision Date2023-04-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Konicaminolta DI-X1 is the device name listed in this FDA 510(k) record. The listed applicant is Konica Minolta, Inc.. It received FDA 510(k) clearance on 2023-04-25 under 510(k) number K230906. 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 2023-04-25. The listed applicant is Konica Minolta, Inc.. The 510(k) number is K230906.

When did Konicaminolta DI-X1 receive FDA 510(k) clearance?

Konicaminolta DI-X1 received FDA 510(k) clearance on 2023-04-25, under 510(k) number K230906.

Who is the listed applicant for Konicaminolta DI-X1?

The FDA 510(k) record lists Konica Minolta, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Konica Minolta, Inc. as applicant

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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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