Trachealator— 510(k) K211894

Substantially Equivalent

Disa Medinotec

FDA 510(k) clearance K211894 for Trachealator, Substantially Equivalent on 2021-11-24. Applicant: Disa Medinotec.

Clearance details

Applicant: Disa Medinotec
Product code: Code KTI
Advisory panel: Ear, Nose, Throat
Date received: 2021-06-21
Decision date: 2021-11-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Johannesburg, ZA

Download summary PDF View on FDA.gov ↗

Adverse events under product code KTI

product code KTI

Malfunction: 642
Total: 642

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.