ADVANCE MODEL UDS-ADV— 510(k) K931574

Name: FDA 510(k) clearance K931574
Creator: U.S. Food and Drug Administration
Published: 1993-08-05

Substantially Equivalent

Laborie Medical Technologies, Ltd.

FDA 510(k) clearance K931574 for ADVANCE MODEL UDS-ADV, Substantially Equivalent on 1993-08-05. Applicant: Laborie Medical Technologies, Ltd.. Device class: 2.

Clearance details

Applicant: Laborie Medical Technologies, Ltd.
Product code: Code EXQ
Device class: Class 2
Regulation: 21 CFR 876.1620
Advisory panel: Gastroenterology, Urology
Date received: 1993-03-30
Decision date: 1993-08-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mississauga, CA

Download summary PDF View on FDA.gov ↗

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