5300 PERCUSSOR— 510(k) K790675

Substantially Equivalent

Hudson Oxygen Therapy Sales Co.

FDA 510(k) clearance K790675 for 5300 PERCUSSOR, Substantially Equivalent on 1979-04-18. Applicant: Hudson Oxygen Therapy Sales Co..

Clearance details

Applicant: Hudson Oxygen Therapy Sales Co.
Product code: Code BYI
Advisory panel: Anesthesiology
Date received: 1979-04-09
Decision date: 1979-04-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code BYI

product code BYI

Death: 3
Total: 3

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.