MATRIX ELECDT & VACUPULLS— 510(k) K930264

Name: FDA 510(k) clearance K930264
Creator: U.S. Food and Drug Administration
Published: 1993-06-29

Substantially Equivalent

Matrix Electromedical, Inc.

FDA 510(k) clearance K930264 for MATRIX ELECDT & VACUPULLS, Substantially Equivalent on 1993-06-29. 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: 1993-06-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Las Vegas, NV, US

Download summary PDF View on FDA.gov ↗

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