Insight Essentials DRF Digital Imaging System
K-Number: K191310 · 2019-06-10
Device Summary
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.
Related Clinical Trials
Related PubMed Literature
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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.