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FDA 510(k)

MOVES

K-Number: K093261 · 2010-03-26

ApplicantThornhill Research, Inc.
Decision Date2010-03-26
Product CodeBTL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MOVES is the device name listed in this FDA 510(k) record. The listed applicant is Thornhill Research, Inc.. It received FDA 510(k) clearance on 2010-03-26 under 510(k) number K093261. 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?

MOVES is a medical device that received FDA 510(k) clearance on 2010-03-26. The listed applicant is Thornhill Research, Inc.. The 510(k) number is K093261.

When did MOVES receive FDA 510(k) clearance?

MOVES received FDA 510(k) clearance on 2010-03-26, under 510(k) number K093261.

Who is the listed applicant for MOVES?

The FDA 510(k) record lists Thornhill Research, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOVES?

The FDA product code for MOVES is BTL.

Related Clinical Trials

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Other records listing Thornhill Research, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K161420MOVES SLC

Related Devices (Code: BTL)

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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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