UROCOMP MODEL 1404— 510(k) K821939

Substantially Equivalent

Life-Tech Intl., Inc.

FDA 510(k) clearance K821939 for UROCOMP MODEL 1404, Substantially Equivalent on 1982-07-13. Applicant: Life-Tech Intl., Inc.. Device class: 2.

Clearance details

Applicant: Life-Tech Intl., Inc.
Product code: Code FAP
Device class: Class 2
Regulation: 21 CFR 876.1620
Advisory panel: Gastroenterology, Urology
Date received: 1982-06-29
Decision date: 1982-07-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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