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FDA 510(k)

Siberian Fit

K-Number: K172439 · 2018-02-14

ApplicantVydence
Decision Date2018-02-14
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Siberian Fit is a medical device manufactured by Vydence. It received FDA 510(k) clearance on 2018-02-14 under approval number K172439. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Siberian Fit?

Siberian Fit is a medical device that received FDA 510(k) clearance on 2018-02-14. It is manufactured by Vydence. The 510(k) number is K172439.

When was Siberian Fit approved by the FDA?

Siberian Fit received FDA 510(k) clearance on 2018-02-14, under approval number K172439.

What company makes Siberian Fit?

Siberian Fit is manufactured by Vydence.

What is the FDA product code for Siberian Fit?

The FDA product code for Siberian Fit is GEX. This falls under the Gastroenterology category.

Related Devices (Code: GEX)

Official Source

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