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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 a medical device manufactured by Invent Medical Corporation. It received FDA 510(k) clearance on 2024-06-14 under approval 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. It is manufactured by Invent Medical Corporation. The 510(k) number is K233707.

When was HFT150 approved by the FDA?

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

What company makes HFT150?

HFT150 is manufactured by Invent Medical Corporation.

What is the FDA product code for HFT150?

The FDA product code for HFT150 is BTT.

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Official Source

View on FDA Database →

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

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