MANIFOLD, UNIVERSAL I.P.P.B— 510(k) K790152

Substantially Equivalent

Airlife, Inc.

FDA 510(k) clearance K790152 for MANIFOLD, UNIVERSAL I.P.P.B, Substantially Equivalent on 1979-03-07. Applicant: Airlife, Inc..

Clearance details

Applicant: Airlife, Inc.
Product code: Code CAF
Advisory panel: Anesthesiology
Date received: 1979-01-12
Decision date: 1979-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.