NEMECTRODYN MODEL 2 & ENDOVAC 2— 510(k) K854721

Name: FDA 510(k) clearance K854721
Creator: U.S. Food and Drug Administration
Published: 1986-03-06

Substantially Equivalent

Nemectron Medical, Inc.

FDA 510(k) clearance K854721 for NEMECTRODYN MODEL 2 & ENDOVAC 2, Substantially Equivalent on 1986-03-06. Applicant: Nemectron Medical, Inc.. Device class: 2.

Clearance details

Applicant: Nemectron Medical, Inc.
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1985-11-22
Decision date: 1986-03-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Temecula, CA, US

Download summary PDF View on FDA.gov ↗

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