RELAXPLUS— 510(k) K951213

Substantially Equivalent

Ultramind International , Ltd.

FDA 510(k) clearance K951213 for RELAXPLUS, Substantially Equivalent on 1995-09-20. Applicant: Ultramind International , Ltd.. Device class: 2.

Clearance details

Applicant: Ultramind International , Ltd.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1995-03-17
Decision date: 1995-09-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eilat, IL

Download summary PDF View on FDA.gov ↗

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