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FDA 510(k)

Instalief

K-Number: K172358 · 2018-01-10

ApplicantPrivi Medical Pte, Ltd.
Decision Date2018-01-10
Product CodeLKX
DecisionSubstantially Equivalent

Device Summary

Instalief is a medical device manufactured by Privi Medical Pte, Ltd.. It received FDA 510(k) clearance on 2018-01-10 under approval number K172358. The device is classified under product code LKX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Instalief?

Instalief is a medical device that received FDA 510(k) clearance on 2018-01-10. It is manufactured by Privi Medical Pte, Ltd.. The 510(k) number is K172358.

When was Instalief approved by the FDA?

Instalief received FDA 510(k) clearance on 2018-01-10, under approval number K172358.

What company makes Instalief?

Instalief is manufactured by Privi Medical Pte, Ltd..

What is the FDA product code for Instalief?

The FDA product code for Instalief is LKX.

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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