PROBLOC INSULATED NEEDLES— 510(k) K926349

Name: FDA 510(k) clearance K926349
Creator: U.S. Food and Drug Administration
Published: 1993-07-29

Substantially Equivalent

Life-Tech Intl., Inc.

FDA 510(k) clearance K926349 for PROBLOC INSULATED NEEDLES, Substantially Equivalent on 1993-07-29. Applicant: Life-Tech Intl., Inc.. Device class: 2.

Clearance details

Applicant: Life-Tech Intl., Inc.
Product code: Code GXZ
Device class: Class 2
Regulation: 21 CFR 882.1350
Advisory panel: Neurology
Date received: 1992-12-17
Decision date: 1993-07-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

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