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FDA 510(k)

HFT150

K-Number: K233707 · 2024-06-14

ApplicantInvent Medical Corporation
Decision Date2024-06-14
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

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.

Frequently Asked Questions

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.

Related Devices (Code: BTT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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