URODEC 500— 510(k) K890284

Substantially Equivalent

Ferguson Medical

FDA 510(k) clearance K890284 for URODEC 500, Substantially Equivalent on 1989-05-30. Applicant: Ferguson Medical. Device class: 2.

Clearance details

Applicant: Ferguson Medical
Product code: Code FES
Device class: Class 2
Regulation: 21 CFR 876.1725
Advisory panel: Gastroenterology, Urology
Date received: 1989-01-19
Decision date: 1989-05-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chico, CA, US

Download summary PDF View on FDA.gov ↗

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