FDA 510(k)

바비 (폴리막론) 일일 착용 소프트 (수용성) 컨택 렌즈

K-번호: K220143 · 2022-09-08

신청자Shenzhen Dashicheng Optical Technology Co., Ltd.

결정일2022-09-08

제품 코드LPL

자문 위원회의료장비 규제 텍스트 번역 OP

결정대체적으로 동일

기기 요약

BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Dashicheng Optical Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-09-08 under 510(k) number K220143. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens?

BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens is a medical device that received FDA 510(k) clearance on 2022-09-08. The listed applicant is Shenzhen Dashicheng Optical Technology Co., Ltd.. The 510(k) number is K220143.

When did BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens receive FDA 510(k) clearance?

BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens received FDA 510(k) clearance on 2022-09-08, under 510(k) number K220143.

Who is the listed applicant for BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens?

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

What is the FDA product code for BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens?

The FDA product code for BARBIE (polymacon) Daily Wear Soft (Hydrophilic) Contact Lens is LPL.

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바비 (폴리막론) 일일 착용 소프트 (수용성) 컨택 렌즈

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: LPL)

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