FDA 510(k)

Motion Correction System

K-번호: K193324 · 2020-02-04

결정일2020-02-04

제품 코드LNH

자문 위원회RA

결정Substantially Equivalent

기기 요약

Motion Correction System is the device name listed in this FDA 510(k) record. The listed applicant is Kineticor, Inc.. It received FDA 510(k) clearance on 2020-02-04 under 510(k) number K193324. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Motion Correction System?

Motion Correction System is a medical device that received FDA 510(k) clearance on 2020-02-04. The listed applicant is Kineticor, Inc.. The 510(k) number is K193324.

When did Motion Correction System receive FDA 510(k) clearance?

Motion Correction System received FDA 510(k) clearance on 2020-02-04, under 510(k) number K193324.

Who is the listed applicant for Motion Correction System?

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

What is the FDA product code for Motion Correction System?

The FDA product code for Motion Correction System is LNH.

공식 출처

FDA 데이터베이스에서 보기 →

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

Motion Correction System

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: LNH)

공식 출처