ATAD ARD CATHETER— 510(k) K040625

Substantially Equivalent

Atad Developments , Ltd.

FDA 510(k) clearance K040625 for ATAD ARD CATHETER, Substantially Equivalent on 2005-01-18. Applicant: Atad Developments , Ltd.. Device class: 2.

Clearance details

Applicant: Atad Developments , Ltd.
Product code: Code HDY
Device class: Class 2
Regulation: 21 CFR 884.4260
Advisory panel: Obstetrics/Gynecology
Date received: 2004-03-09
Decision date: 2005-01-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Haifa, IL

Download summary PDF View on FDA.gov ↗

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