CURITY FIBEROPTIC INTUBATING AIRWAY— 510(k) K855137

Substantially Equivalent

The Kendal Co.

FDA 510(k) clearance K855137 for CURITY FIBEROPTIC INTUBATING AIRWAY, Substantially Equivalent on 1986-03-11. Applicant: The Kendal Co..

Clearance details

Applicant: The Kendal Co.
Product code: Code CAE
Advisory panel: Anesthesiology
Date received: 1985-12-23
Decision date: 1986-03-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boston, MA, US

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Adverse events under product code CAE

product code CAE

Death: 4
Total: 4

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.