FDA 510(k)

SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses

K-번호: K241398 · 2024-10-22

신청자Tianjin Mastervision Technology Co., Ltd.

결정일2024-10-22

제품 코드HQD

자문 위원회OP

결정Substantially Equivalent

기기 요약

SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses is the device name listed in this FDA 510(k) record. The listed applicant is Tianjin Mastervision Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-10-22 under 510(k) number K241398. The device is classified under product code HQD. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses?

SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses is a medical device that received FDA 510(k) clearance on 2024-10-22. The listed applicant is Tianjin Mastervision Technology Co., Ltd.. The 510(k) number is K241398.

When did SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses receive FDA 510(k) clearance?

SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses received FDA 510(k) clearance on 2024-10-22, under 510(k) number K241398.

Who is the listed applicant for SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses?

The FDA 510(k) record lists Tianjin Mastervision Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses?

The FDA product code for SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses is HQD.

공식 출처

FDA 데이터베이스에서 보기 →

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

SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: HQD)

공식 출처