MOTION WATCH AND PRO-DIARY— 510(k) K132764

Substantially Equivalent

Camntech, Ltd.

FDA 510(k) clearance K132764 for MOTION WATCH AND PRO-DIARY, Substantially Equivalent on 2014-01-21. Applicant: Camntech, Ltd.. Device class: 2.

Clearance details

Applicant: Camntech, Ltd.
Product code: Code LEL
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 2013-09-04
Decision date: 2014-01-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Papworth Everard, Cambridgeshire, GB

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.