ELECTRONEURAL STIMULATOR 12— 510(k) K831487

Substantially Equivalent

Meridia 12 Corp.

FDA 510(k) clearance K831487 for ELECTRONEURAL STIMULATOR 12, Substantially Equivalent on 1983-10-28. Applicant: Meridia 12 Corp.. Device class: 2.

Clearance details

Applicant: Meridia 12 Corp.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1983-05-10
Decision date: 1983-10-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, 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.