FDA 510(k)

i-STAT G3+ cartridge with the i-STAT 1 System

K番号: K223857 · 2023-09-15

決定日2023-09-15

製品コードCHL

諮問委員会CH 当社の医療機器は、FDA（米国食品医薬品局）の規制に従って製造・販売されています。製品は、510(k)通知書およびPMA（プレマーケティング評価）を通じて承認を受けています。臨床試験情報は、NCT（臨床試験登録番号）およびPMID（PubMed ID）で確認できます。詳細については、以下のURLをご参照ください。 [URL]

決定大幅同等

医療機器の概要

i-STAT G3+ cartridge with the i-STAT 1 System is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Point of Care, Inc.. It received FDA 510(k) clearance on 2023-09-15 under 510(k) number K223857. The device is classified under product code CHL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the i-STAT G3+ cartridge with the i-STAT 1 System?

i-STAT G3+ cartridge with the i-STAT 1 System is a medical device that received FDA 510(k) clearance on 2023-09-15. The listed applicant is Abbott Point of Care, Inc.. The 510(k) number is K223857.

When did i-STAT G3+ cartridge with the i-STAT 1 System receive FDA 510(k) clearance?

i-STAT G3+ cartridge with the i-STAT 1 System received FDA 510(k) clearance on 2023-09-15, under 510(k) number K223857.

Who is the listed applicant for i-STAT G3+ cartridge with the i-STAT 1 System?

The FDA 510(k) record lists Abbott Point of Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for i-STAT G3+ cartridge with the i-STAT 1 System?

The FDA product code for i-STAT G3+ cartridge with the i-STAT 1 System is CHL.

申請者としてAbbott Point of Care, Inc.を記載するその他の記録

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