NULIFE— 510(k) K962837

Name: FDA 510(k) clearance K962837
Creator: U.S. Food and Drug Administration
Published: 1996-10-02

Substantially Equivalent

Med-Tech Rubber & Engineering Industries

FDA 510(k) clearance K962837 for NULIFE, Substantially Equivalent on 1996-10-02. Applicant: Med-Tech Rubber & Engineering Industries. Device class: 1.

Clearance details

Applicant: Med-Tech Rubber & Engineering Industries
Product code: Code KGO
Device class: Class 1
Regulation: 21 CFR 878.4460
Advisory panel: General, Plastic Surgery
Date received: 1996-07-09
Decision date: 1996-10-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sussex Rad, Yculla,, IN

Download summary PDF View on FDA.gov ↗

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