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FDA 510(k)

ImagePilot

K-Number: K210066 · 2021-05-06

ApplicantKonica Minolta, Inc.
Decision Date2021-05-06
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ImagePilot is a medical device manufactured by Konica Minolta, Inc.. It received FDA 510(k) clearance on 2021-05-06 under approval number K210066. 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 ImagePilot?

ImagePilot is a medical device that received FDA 510(k) clearance on 2021-05-06. It is manufactured by Konica Minolta, Inc.. The 510(k) number is K210066.

When was ImagePilot approved by the FDA?

ImagePilot received FDA 510(k) clearance on 2021-05-06, under approval number K210066.

What company makes ImagePilot?

ImagePilot is manufactured by Konica Minolta, Inc..

What is the FDA product code for ImagePilot?

The FDA product code for ImagePilot 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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