DISCOSCOPES, CERVICAL ENDOSCOPES— 510(k) K130778

Substantially Equivalent

Rz Medizintechnik GmbH

FDA 510(k) clearance K130778 for DISCOSCOPES, CERVICAL ENDOSCOPES, Substantially Equivalent on 2014-04-14. Applicant: Rz Medizintechnik GmbH.

Clearance details

Applicant: Rz Medizintechnik GmbH
Product code: Code HRX
Advisory panel: Orthopedic
Date received: 2013-03-21
Decision date: 2014-04-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mühlheim An Der Donau, DE

Download summary PDF View on FDA.gov ↗

Adverse events under product code HRX

product code HRX

Injury: 623
Malfunction: 11,257
Total: 11,880

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.