MEDISONIC HUMDIFIER/INHALER— 510(k) K901114

Substantially Equivalent

Medisonic U.S.A., Inc.

FDA 510(k) clearance K901114 for MEDISONIC HUMDIFIER/INHALER, Substantially Equivalent on 1990-05-22. Applicant: Medisonic U.S.A., Inc..

Clearance details

Applicant: Medisonic U.S.A., Inc.
Product code: Code CAF
Advisory panel: Anesthesiology
Date received: 1990-03-07
Decision date: 1990-05-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clarence, NY, US

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Adverse events under product code CAF

product code CAF

Death: 22
Injury: 125
Malfunction: 613
Other: 11
Total: 771

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.