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FDA 510(k)

Lariat, Hot/Cold Snare

K-Number: K200745 · 2020-04-21

ApplicantUnited States Endoscopy Group, Inc.
Decision Date2020-04-21
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Lariat, Hot/Cold Snare is a medical device manufactured by United States Endoscopy Group, Inc.. It received FDA 510(k) clearance on 2020-04-21 under approval number K200745. The device is classified under product code FDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Lariat, Hot/Cold Snare?

Lariat, Hot/Cold Snare is a medical device that received FDA 510(k) clearance on 2020-04-21. It is manufactured by United States Endoscopy Group, Inc.. The 510(k) number is K200745.

When was Lariat, Hot/Cold Snare approved by the FDA?

Lariat, Hot/Cold Snare received FDA 510(k) clearance on 2020-04-21, under approval number K200745.

What company makes Lariat, Hot/Cold Snare?

Lariat, Hot/Cold Snare is manufactured by United States Endoscopy Group, Inc..

What is the FDA product code for Lariat, Hot/Cold Snare?

The FDA product code for Lariat, Hot/Cold Snare is FDI.

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Related Devices (Code: FDI)

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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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