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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 the device name listed in this FDA 510(k) record. The listed applicant is Konica Minolta, Inc.. It received FDA 510(k) clearance on 2021-09-13 under 510(k) 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. The listed applicant is Konica Minolta, Inc.. The 510(k) number is K212685.

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

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

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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Related Devices (Code: 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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