FDA 510(k)

MedicCO2LON (MedicCO2LON)

K-번호: K240847 · 2024-10-30

결정일2024-10-30

제품 코드FCX

자문 위원회GU

결정Substantially Equivalent

기기 요약

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

자주 묻는 질문

What is the MedicCO2LON (MedicCO2LON)?

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

When did MedicCO2LON (MedicCO2LON) receive FDA 510(k) clearance?

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

Who is the listed applicant for MedicCO2LON (MedicCO2LON)?

The FDA 510(k) record lists Ide Vision, Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

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

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MedicCO2LON (MedicCO2LON)

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: FCX)

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