MODIFIED LEVEEN NEEDLE ELECTRODE— 510(k) K962313

Name: FDA 510(k) clearance K962313
Creator: U.S. Food and Drug Administration
Published: 1996-09-11

Substantially Equivalent

Radiotherapeutics Corp.

FDA 510(k) clearance K962313 for MODIFIED LEVEEN NEEDLE ELECTRODE, Substantially Equivalent on 1996-09-11. Applicant: Radiotherapeutics Corp.. Device class: 2.

Clearance details

Applicant: Radiotherapeutics Corp.
Product code: Code JOS
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 1996-06-17
Decision date: 1996-09-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mountain View, CA, US

Download summary PDF View on FDA.gov ↗

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