Ritleng®+ and Ritleng®+ PVP— 510(k) K201892

Name: FDA 510(k) clearance K201892
Creator: U.S. Food and Drug Administration
Published: 2021-03-11

Substantially Equivalent

Fci (France Chirurgie Instrumentation) Sas

FDA 510(k) clearance K201892 for Ritleng®+ and Ritleng®+ PVP, Substantially Equivalent on 2021-03-11. Applicant: Fci (France Chirurgie Instrumentation) Sas. Device class: Unclassified.

Clearance details

Applicant: Fci (France Chirurgie Instrumentation) Sas
Product code: Code OKS
Device class: Unclassified
Advisory panel: Unknown
Date received: 2020-07-08
Decision date: 2021-03-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paris, FR

Download summary PDF View on FDA.gov ↗

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