FDA 510(k)

オムニポッド®インスリン管理システム、オムニポッドDASH®インスリン管理システム

K番号: K211575 · 2021-08-13

決定日2021-08-13

製品コードLZG

諮問委員会医療機器規制テキストの翻訳は以下の通りです。 HO [翻訳が提供されなかったため、原文の「HO」がそのまま使用されます]

決定大幅同等

医療機器の概要

Omnipod® Insulin Management System, Omnipod DASH® Insulin Management System is the device name listed in this FDA 510(k) record. The listed applicant is Insulet Corporation. It received FDA 510(k) clearance on 2021-08-13 under 510(k) number K211575. The device is classified under product code LZG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Omnipod® Insulin Management System, Omnipod DASH® Insulin Management System?

Omnipod® Insulin Management System, Omnipod DASH® Insulin Management System is a medical device that received FDA 510(k) clearance on 2021-08-13. The listed applicant is Insulet Corporation. The 510(k) number is K211575.

When did Omnipod® Insulin Management System, Omnipod DASH® Insulin Management System receive FDA 510(k) clearance?

Omnipod® Insulin Management System, Omnipod DASH® Insulin Management System received FDA 510(k) clearance on 2021-08-13, under 510(k) number K211575.

Who is the listed applicant for Omnipod® Insulin Management System, Omnipod DASH® Insulin Management System?

The FDA 510(k) record lists Insulet Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Omnipod® Insulin Management System, Omnipod DASH® Insulin Management System?

The FDA product code for Omnipod® Insulin Management System, Omnipod DASH® Insulin Management System is LZG.

申請者としてInsulet Corporationを記載するその他の記録

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公式ソース

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