FDA 510(k)

AMD Anti-Fog Solution

K番号: K181887 · 2019-01-22

決定日2019-01-22

製品コードOCT

諮問委員会以下は、指定された医療機器規制テキストの日本語訳です。以下の医療機器規制テキストを日本語に翻訳してください。会社名、製品名、FDA、510(k)、PMA、NCT、PMID、識別子、およびURLを保護してください。ポリシー：medical-regulatory-v1 [原文] GU [翻訳] GU

決定大幅同等

医療機器の概要

AMD Anti-Fog Solution is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Medical Design Co., Ltd.. It received FDA 510(k) clearance on 2019-01-22 under 510(k) number K181887. The device is classified under product code OCT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the AMD Anti-Fog Solution?

AMD Anti-Fog Solution is a medical device that received FDA 510(k) clearance on 2019-01-22. The listed applicant is Advanced Medical Design Co., Ltd.. The 510(k) number is K181887.

When did AMD Anti-Fog Solution receive FDA 510(k) clearance?

AMD Anti-Fog Solution received FDA 510(k) clearance on 2019-01-22, under 510(k) number K181887.

Who is the listed applicant for AMD Anti-Fog Solution?

The FDA 510(k) record lists Advanced Medical Design Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMD Anti-Fog Solution?

The FDA product code for AMD Anti-Fog Solution is OCT.

申請者としてAdvanced Medical Design Co., Ltd.を記載するその他の記録

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