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FDA 510(k)

AliTight

K-Number: K231146 · 2023-09-08

ApplicantAlic Iotech, LLC
Decision Date2023-09-08
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AliTight is a medical device manufactured by Alic Iotech, LLC. It received FDA 510(k) clearance on 2023-09-08 under approval number K231146. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AliTight?

AliTight is a medical device that received FDA 510(k) clearance on 2023-09-08. It is manufactured by Alic Iotech, LLC. The 510(k) number is K231146.

When was AliTight approved by the FDA?

AliTight received FDA 510(k) clearance on 2023-09-08, under approval number K231146.

What company makes AliTight?

AliTight is manufactured by Alic Iotech, LLC.

What is the FDA product code for AliTight?

The FDA product code for AliTight is GEI.

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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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