BIVONA FLEXTEND PEDIATRIC & NEONATAL TRACHEOSTROMY TUBES— 510(k) K944178

Substantially Equivalent

Bivona Medical Technologies

FDA 510(k) clearance K944178 for BIVONA FLEXTEND PEDIATRIC & NEONATAL TRACHEOSTROMY TUBES, Substantially Equivalent on 1994-10-27. Applicant: Bivona Medical Technologies.

Clearance details

Applicant: Bivona Medical Technologies
Product code: Code JOH
Advisory panel: Anesthesiology
Date received: 1994-08-26
Decision date: 1994-10-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gary, IN, US

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Adverse events under product code JOH

product code JOH

Death: 42
Injury: 1,344
Malfunction: 5,608
Other: 1
Total: 6,995

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.