MATRIX PRO-ELECDT— 510(k) K930263

Substantially Equivalent

Matrix Electromedical, Inc.

FDA 510(k) clearance K930263 for MATRIX PRO-ELECDT, Substantially Equivalent on 1994-06-09. Applicant: Matrix Electromedical, Inc.. Device class: 2.

Clearance details

Applicant: Matrix Electromedical, Inc.
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1993-01-19
Decision date: 1994-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Las Vegas, NV, US

Download summary PDF View on FDA.gov ↗

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More clearances from Matrix Electromedical, Inc.

K930264 — MATRIX ELECDT & VACUPULLS1993-06-29

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