FDA 510(k)

ImagePilot

K-Number: K210066 · 2021-05-06

Decision Date2021-05-06

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

ImagePilot 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 2021-05-06 under 510(k) 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. The listed applicant is Konica Minolta, Inc.. The 510(k) number is K210066.

When did ImagePilot receive FDA 510(k) clearance?

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

Who is the listed applicant for ImagePilot?

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 ImagePilot?

The FDA product code for ImagePilot is LLZ.

Other records listing Konica Minolta, Inc. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.