POLYVUE (polymacon) 软性(亲水性)隐形眼镜,POLYVUE COLOR (polymacon) 软性(亲水性)隐形眼镜
K号: K221517 · 2022-10-04
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器械摘要
常见问题
What is the POLYVUE (polymacon) Soft (hydrophilic) Contact Lens, POLYVUE COLOR (polymacon) Soft (hydrophilic) Contact Lens?
POLYVUE (polymacon) Soft (hydrophilic) Contact Lens, POLYVUE COLOR (polymacon) Soft (hydrophilic) Contact Lens is a medical device that received FDA 510(k) clearance on 2022-10-04. The listed applicant is INTEROJO, Inc.. The 510(k) number is K221517.
When did POLYVUE (polymacon) Soft (hydrophilic) Contact Lens, POLYVUE COLOR (polymacon) Soft (hydrophilic) Contact Lens receive FDA 510(k) clearance?
POLYVUE (polymacon) Soft (hydrophilic) Contact Lens, POLYVUE COLOR (polymacon) Soft (hydrophilic) Contact Lens received FDA 510(k) clearance on 2022-10-04, under 510(k) number K221517.
Who is the listed applicant for POLYVUE (polymacon) Soft (hydrophilic) Contact Lens, POLYVUE COLOR (polymacon) Soft (hydrophilic) Contact Lens?
The FDA 510(k) record lists INTEROJO, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POLYVUE (polymacon) Soft (hydrophilic) Contact Lens, POLYVUE COLOR (polymacon) Soft (hydrophilic) Contact Lens?
The FDA product code for POLYVUE (polymacon) Soft (hydrophilic) Contact Lens, POLYVUE COLOR (polymacon) Soft (hydrophilic) Contact Lens is LPL.
相关临床试验
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列明INTEROJO, Inc.为申报人的其他记录
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
相关器械(代码:LPL)
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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