LIFELINES PHOTIC STIMULATOR— 510(k) K101691

Substantially Equivalent

Lifelines , Ltd.

FDA 510(k) clearance K101691 for LIFELINES PHOTIC STIMULATOR, Substantially Equivalent on 2010-08-10. Applicant: Lifelines , Ltd.. Device class: 2.

Clearance details

Applicant: Lifelines , Ltd.
Product code: Code GWE
Device class: Class 2
Regulation: 21 CFR 882.1890
Advisory panel: Neurology
Date received: 2010-06-16
Decision date: 2010-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Crofton, MD, US

Download summary PDF View on FDA.gov ↗

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