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FDA 510(k)

AIE REGION OF INTEREST IMAGE ENHANCEMENT

K-Number: K062059 · 2006-09-06

ApplicantAdvanced Image Enhancement
Decision Date2006-09-06
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AIE REGION OF INTEREST IMAGE ENHANCEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Image Enhancement. It received FDA 510(k) clearance on 2006-09-06 under 510(k) number K062059. 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 AIE REGION OF INTEREST IMAGE ENHANCEMENT?

AIE REGION OF INTEREST IMAGE ENHANCEMENT is a medical device that received FDA 510(k) clearance on 2006-09-06. The listed applicant is Advanced Image Enhancement. The 510(k) number is K062059.

When did AIE REGION OF INTEREST IMAGE ENHANCEMENT receive FDA 510(k) clearance?

AIE REGION OF INTEREST IMAGE ENHANCEMENT received FDA 510(k) clearance on 2006-09-06, under 510(k) number K062059.

Who is the listed applicant for AIE REGION OF INTEREST IMAGE ENHANCEMENT?

The FDA 510(k) record lists Advanced Image Enhancement as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIE REGION OF INTEREST IMAGE ENHANCEMENT?

The FDA product code for AIE REGION OF INTEREST IMAGE ENHANCEMENT is LLZ.

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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.

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