CAPNOSTREAM20 TWO PARAMETER BEDSIDE MONITOR & CAPNOSTREAM10 ONE PARAMETER BEDSIDE MONITOR— 510(k) K060065

Substantially Equivalent

Oridion Capnography, Inc.

FDA 510(k) clearance K060065 for CAPNOSTREAM20 TWO PARAMETER BEDSIDE MONITOR & CAPNOSTREAM10 ONE PARAMETER BEDSIDE MONITOR, Substantially Equivalent on 2006-05-04. Applicant: Oridion Capnography, Inc..

Clearance details

Applicant: Oridion Capnography, Inc.
Product code: Code DQA
Advisory panel: Cardiovascular
Date received: 2006-01-09
Decision date: 2006-05-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jerusalem, IL

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.