NASOPHARYNGOSCOPE, BRONCHOSCOPE— 510(k) K070580

Substantially Equivalent

Xion GmbH

FDA 510(k) clearance K070580 for NASOPHARYNGOSCOPE, BRONCHOSCOPE, Substantially Equivalent on 2007-06-13. Applicant: Xion GmbH.

Clearance details

Applicant: Xion GmbH
Product code: Code EOB
Advisory panel: Ear, Nose, Throat
Date received: 2007-03-01
Decision date: 2007-06-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Berlin, DE

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Adverse events under product code EOB

product code EOB

Malfunction: 6,143
Total: 6,143

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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