FDA 510(k)

MOVES SLC

Numéro K : K161420 · 2017-06-06

Date de décision2017-06-06

Code produitBTL

Comité consultatifAN

DécisionSubstantially Equivalent

Résumé du dispositif

MOVES SLC 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 2017-06-06 under 510(k) number K161420. The device is classified under product code BTL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the MOVES SLC?

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

When did MOVES SLC receive FDA 510(k) clearance?

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

Who is the listed applicant for MOVES SLC?

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 SLC?

The FDA product code for MOVES SLC is BTL.

Essais cliniques associés

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Source officielle

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