Epidural MiniFilter LUER 80369-7, Epidural MiniFilter NRFit 80369-6— 510(k) K190663

Name: FDA 510(k) clearance K190663
Creator: U.S. Food and Drug Administration
Published: 2019-06-17

Substantially Equivalent

PAJUNK GmbH Medizintechnologie

FDA 510(k) clearance K190663 for Epidural MiniFilter LUER 80369-7, Epidural MiniFilter NRFit 80369-6, Substantially Equivalent on 2019-06-17. Applicant: PAJUNK GmbH Medizintechnologie. Device class: 2.

Clearance details

Applicant: PAJUNK GmbH Medizintechnologie
Product code: Code BSN
Device class: Class 2
Regulation: 21 CFR 868.5130
Advisory panel: Anesthesiology
Date received: 2019-03-15
Decision date: 2019-06-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Geisingen, DE

Download summary PDF View on FDA.gov ↗

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