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FDA 510(k)

Konicaminolta DI-X1

K-Number: K182431 · 2018-11-26

ApplicantKonica Minolta, Inc.
Decision Date2018-11-26
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 2018-11-26 under approval number K182431. 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 2018-11-26. It is manufactured by Konica Minolta, Inc.. The 510(k) number is K182431.

When was Konicaminolta DI-X1 approved by the FDA?

Konicaminolta DI-X1 received FDA 510(k) clearance on 2018-11-26, under approval number K182431.

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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