FDA 510(k)

EliA Ro52, EliA Ro60

K号: K210902 · 2022-07-27

决定日期2022-07-27

产品代码LKJ

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决定实质等同

器械摘要

EliA Ro52, EliA Ro60 is the device name listed in this FDA 510(k) record. The listed applicant is Phadia AB. It received FDA 510(k) clearance on 2022-07-27 under 510(k) number K210902. The device is classified under product code LKJ. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the EliA Ro52, EliA Ro60?

EliA Ro52, EliA Ro60 is a medical device that received FDA 510(k) clearance on 2022-07-27. The listed applicant is Phadia AB. The 510(k) number is K210902.

When did EliA Ro52, EliA Ro60 receive FDA 510(k) clearance?

EliA Ro52, EliA Ro60 received FDA 510(k) clearance on 2022-07-27, under 510(k) number K210902.

Who is the listed applicant for EliA Ro52, EliA Ro60?

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 EliA Ro52, EliA Ro60?

The FDA product code for EliA Ro52, EliA Ro60 is LKJ.

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。

K253367EliA CTD 13 屏幕检测 K212181ImmunoCAP 过敏原 f433，过敏原成分 rTri a 14 LTP，小麦，ImmunoCAP 过敏原 f416，过敏原成分 rTri a 19 Omega-5 谷蛋白，小麦，ImmunoCAP 过敏原 f449，过敏原成分 rSes i 1 芝麻籽 K202540EliA Rib-P K202541EliA RNA Pol III K202067EliA SmDP-S K200279ImmunoCAP 过敏原 o215，成分 nGal-alpha-1,3-Gal(alpha-Gal) 甲状腺球蛋白，牛

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