OHMEDA INOVENT DELIVERY SYSTEM— 510(k) DEN000001

Unknown

Ohmeda Medical

FDA 510(k) clearance DEN000001 for OHMEDA INOVENT DELIVERY SYSTEM, Unknown on 2000-01-11. Applicant: Ohmeda Medical.

Clearance details

Applicant: Ohmeda Medical
Product code: Code MRN
Advisory panel: Anesthesiology
Date received: 2000-01-07
Decision date: 2000-01-11
Decision: Unknown
Clearance type: Post-NSE
Location: Madison, WI, US

View on FDA.gov ↗

Adverse events under product code MRN

product code MRN

Death: 9
Malfunction: 910
Total: 919

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.