VALVE, PEEP— 510(k) K760230

Substantially Equivalent

Ohio Medical Products

FDA 510(k) clearance K760230 for VALVE, PEEP, Substantially Equivalent on 1976-08-06. Applicant: Ohio Medical Products.

Clearance details

Applicant: Ohio Medical Products
Product code: Code BYE
Advisory panel: Anesthesiology
Date received: 1976-07-14
Decision date: 1976-08-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.