PROBLOC INSULATED NEEDLES— 510(k) K926349

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..

Clearance details

Applicant: Life-Tech Intl., Inc.
Product code: Code GXZ
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 ↗

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