OHMEDA HAND HELD OXIMETER— 510(k) K931304

Substantially Equivalent

Ohmeda Medical

FDA 510(k) clearance K931304 for OHMEDA HAND HELD OXIMETER, Substantially Equivalent on 1994-09-29. Applicant: Ohmeda Medical.

Clearance details

Applicant: Ohmeda Medical
Product code: Code DQA
Advisory panel: Cardiovascular
Date received: 1993-03-15
Decision date: 1994-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Louisville, CO, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DQA

product code DQA

Death: 66
Malfunction: 2,867
Other: 1
Total: 2,934

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.