PEEP VALVE— 510(k) K902062

Substantially Equivalent

Hudson Oxygen Therapy Sales Co.

FDA 510(k) clearance K902062 for PEEP VALVE, Substantially Equivalent on 1990-09-04. Applicant: Hudson Oxygen Therapy Sales Co..

Clearance details

Applicant: Hudson Oxygen Therapy Sales Co.
Product code: Code BYE
Advisory panel: Anesthesiology
Date received: 1990-05-08
Decision date: 1990-09-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Temecula, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code BYE

product code BYE

Death: 5
Total: 5

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.