FDA 510(k)

Median LCS (내부 이름) / eyonis LCS (상표명) (1.0)

K-번호: K251474 · 2026-02-06

결정일2026-02-06

제품 코드QDQ

자문 위원회RA

결정Substantially Equivalent

기기 요약

Median LCS (internal name) / eyonis LCS (trade name) (1.0) is the device name listed in this FDA 510(k) record. The listed applicant is Median Technologies. It received FDA 510(k) clearance on 2026-02-06 under 510(k) number K251474. The device is classified under product code QDQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Median LCS (internal name) / eyonis LCS (trade name) (1.0)?

Median LCS (internal name) / eyonis LCS (trade name) (1.0) is a medical device that received FDA 510(k) clearance on 2026-02-06. The listed applicant is Median Technologies. The 510(k) number is K251474.

When did Median LCS (internal name) / eyonis LCS (trade name) (1.0) receive FDA 510(k) clearance?

Median LCS (internal name) / eyonis LCS (trade name) (1.0) received FDA 510(k) clearance on 2026-02-06, under 510(k) number K251474.

Who is the listed applicant for Median LCS (internal name) / eyonis LCS (trade name) (1.0)?

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

What is the FDA product code for Median LCS (internal name) / eyonis LCS (trade name) (1.0)?

The FDA product code for Median LCS (internal name) / eyonis LCS (trade name) (1.0) is QDQ.

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Median LCS (내부 이름) / eyonis LCS (상표명) (1.0)

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: QDQ)

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