FDA 510(k)

HFT150

K 號：K233707 · 2024-06-14

決定日期2024-06-14

產品代碼BTT

諮詢委員會AN

決定相當於

器材摘要

HFT150 is the device name listed in this FDA 510(k) record. The listed applicant is Invent Medical Corporation. It received FDA 510(k) clearance on 2024-06-14 under 510(k) number K233707. The device is classified under product code BTT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the HFT150?

HFT150 is a medical device that received FDA 510(k) clearance on 2024-06-14. The listed applicant is Invent Medical Corporation. The 510(k) number is K233707.

When did HFT150 receive FDA 510(k) clearance?

HFT150 received FDA 510(k) clearance on 2024-06-14, under 510(k) number K233707.

Who is the listed applicant for HFT150?

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

What is the FDA product code for HFT150?

The FDA product code for HFT150 is BTT.

相關器械（代碼：BTT）

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官方來源

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