ImmunoCAP过敏原d202,过敏原成分rDer p 1,尘螨
K号: K150597 · 2016-02-29
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器械摘要
常见问题
What is the ImmunoCAP Allergen d202, Allergen component rDer p 1,House dust mite?
ImmunoCAP Allergen d202, Allergen component rDer p 1,House dust mite is a medical device that received FDA 510(k) clearance on 2016-02-29. The listed applicant is Phadia AB. The 510(k) number is K150597.
When did ImmunoCAP Allergen d202, Allergen component rDer p 1,House dust mite receive FDA 510(k) clearance?
ImmunoCAP Allergen d202, Allergen component rDer p 1,House dust mite received FDA 510(k) clearance on 2016-02-29, under 510(k) number K150597.
Who is the listed applicant for ImmunoCAP Allergen d202, Allergen component rDer p 1,House dust mite?
The FDA 510(k) record lists Phadia AB as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ImmunoCAP Allergen d202, Allergen component rDer p 1,House dust mite?
The FDA product code for ImmunoCAP Allergen d202, Allergen component rDer p 1,House dust mite is DHB.
相关临床试验
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列明Phadia AB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:DHB)
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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