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FDA 510(k)

Insight Essentials DRF Digital Imaging System

K-Number: K191310 · 2019-06-10

Decision Date2019-06-10
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Insight Essentials DRF Digital Imaging System is a medical device manufactured by Imaging Engineering, LLC. It received FDA 510(k) clearance on 2019-06-10 under approval number K191310. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Insight Essentials DRF Digital Imaging System?

Insight Essentials DRF Digital Imaging System is a medical device that received FDA 510(k) clearance on 2019-06-10. It is manufactured by Imaging Engineering, LLC. The 510(k) number is K191310.

When was Insight Essentials DRF Digital Imaging System approved by the FDA?

Insight Essentials DRF Digital Imaging System received FDA 510(k) clearance on 2019-06-10, under approval number K191310.

What company makes Insight Essentials DRF Digital Imaging System?

Insight Essentials DRF Digital Imaging System is manufactured by Imaging Engineering, LLC.

What is the FDA product code for Insight Essentials DRF Digital Imaging System?

The FDA product code for Insight Essentials DRF Digital Imaging System is JAA.

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Official Source

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