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FDA 510(k)

MOVES SLC

K-Number: K161420 · 2017-06-06

ApplicantThornhill Research, Inc.
Decision Date2017-06-06
Product CodeBTL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MOVES SLC is a medical device manufactured by Thornhill Research, Inc.. It received FDA 510(k) clearance on 2017-06-06 under approval number K161420. The device is classified under product code BTL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOVES SLC?

MOVES SLC is a medical device that received FDA 510(k) clearance on 2017-06-06. It is manufactured by Thornhill Research, Inc.. The 510(k) number is K161420.

When was MOVES SLC approved by the FDA?

MOVES SLC received FDA 510(k) clearance on 2017-06-06, under approval number K161420.

What company makes MOVES SLC?

MOVES SLC is manufactured by Thornhill Research, Inc..

What is the FDA product code for MOVES SLC?

The FDA product code for MOVES SLC is BTL.

Other Devices by Thornhill Research, Inc.

DEN170044ClearMate

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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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