DeviceClearance

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

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.

Clearance details

Applicant
PAJUNK GmbH Medizintechnologie
Product code
Code BSN
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Geisingen, DE
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Data sourced from openFDA. This site is unofficial and independent of the FDA.