ANCHORSURE— 510(k) K120831

Substantially Equivalent

Neomedic International S.L.

FDA 510(k) clearance K120831 for ANCHORSURE, Substantially Equivalent on 2012-10-12. Applicant: Neomedic International S.L.. Device class: 2.

Clearance details

Applicant: Neomedic International S.L.
Product code: Code PBQ
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 2012-03-19
Decision date: 2012-10-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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