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FDA 510(k)

MedicCO2LON (MedicCO2LON)

K-Number: K240847 · 2024-10-30

ApplicantIde Vision, Ltd.
Decision Date2024-10-30
Product CodeFCX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MedicCO2LON (MedicCO2LON) is a medical device manufactured by Ide Vision, Ltd.. It received FDA 510(k) clearance on 2024-10-30 under approval number K240847. The device is classified under product code FCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MedicCO2LON (MedicCO2LON)?

MedicCO2LON (MedicCO2LON) is a medical device that received FDA 510(k) clearance on 2024-10-30. It is manufactured by Ide Vision, Ltd.. The 510(k) number is K240847.

When was MedicCO2LON (MedicCO2LON) approved by the FDA?

MedicCO2LON (MedicCO2LON) received FDA 510(k) clearance on 2024-10-30, under approval number K240847.

What company makes MedicCO2LON (MedicCO2LON)?

MedicCO2LON (MedicCO2LON) is manufactured by Ide Vision, Ltd..

What is the FDA product code for MedicCO2LON (MedicCO2LON)?

The FDA product code for MedicCO2LON (MedicCO2LON) is FCX.

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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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