SCHOELLY SINUSCOPE— 510(k) K142249

Substantially Equivalent

Schoelly Fiberoptic GmbH

FDA 510(k) clearance K142249 for SCHOELLY SINUSCOPE, Substantially Equivalent on 2015-01-27. Applicant: Schoelly Fiberoptic GmbH.

Clearance details

Applicant: Schoelly Fiberoptic GmbH
Product code: Code EOB
Advisory panel: Ear, Nose, Throat
Date received: 2014-08-14
Decision date: 2015-01-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denzlingen, DE

Download summary PDF View on FDA.gov ↗

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.