FDA 510(k)

eXaSkin Plus

K-번호: K252784 · 2026-05-22

결정일2026-05-22

제품 코드MUJ

자문 위원회RA

결정Substantially Equivalent

기기 요약

eXaSkin Plus is the device name listed in this FDA 510(k) record. The listed applicant is Anatomical Geometry S.L.. It received FDA 510(k) clearance on 2026-05-22 under 510(k) number K252784. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the eXaSkin Plus?

eXaSkin Plus is a medical device that received FDA 510(k) clearance on 2026-05-22. The listed applicant is Anatomical Geometry S.L.. The 510(k) number is K252784.

When did eXaSkin Plus receive FDA 510(k) clearance?

eXaSkin Plus received FDA 510(k) clearance on 2026-05-22, under 510(k) number K252784.

Who is the listed applicant for eXaSkin Plus?

The FDA 510(k) record lists Anatomical Geometry S.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for eXaSkin Plus?

The FDA product code for eXaSkin Plus is MUJ.

공식 출처

FDA 데이터베이스에서 보기 →

FDA Open API에서 수집된 데이터입니다. 가장 정확하고 공인된 정보는 항상 공식 레코드를 참조하시기 바랍니다.

eXaSkin Plus

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: MUJ)

공식 출처