REBOX II (TENS)— 510(k) K895183

Substantially Equivalent

Rebox (Uk) , Ltd.

FDA 510(k) clearance K895183 for REBOX II (TENS), Substantially Equivalent on 1990-01-19. Applicant: Rebox (Uk) , Ltd.. Device class: 2.

Clearance details

Applicant: Rebox (Uk) , Ltd.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1989-08-11
Decision date: 1990-01-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, 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.