MENTOR 150 PLUS TRANSCUTANEOUS ELEC.— 510(k) K842812

Name: FDA 510(k) clearance K842812
Creator: U.S. Food and Drug Administration
Published: 1984-08-08

Substantially Equivalent

Mentor Corp.

FDA 510(k) clearance K842812 for MENTOR 150 PLUS TRANSCUTANEOUS ELEC., Substantially Equivalent on 1984-08-08. Applicant: Mentor Corp.. Device class: 2.

Clearance details

Applicant: Mentor Corp.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1984-07-18
Decision date: 1984-08-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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