OXYGEN SENSING DEVICE, MODIFICATION— 510(k) K913392

Substantially Equivalent

Devilbiss Health Care, Inc.

FDA 510(k) clearance K913392 for OXYGEN SENSING DEVICE, MODIFICATION, Substantially Equivalent on 1992-07-17. Applicant: Devilbiss Health Care, Inc..

Clearance details

Applicant: Devilbiss Health Care, Inc.
Product code: Code CCL
Advisory panel: Anesthesiology
Date received: 1991-07-29
Decision date: 1992-07-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Somerset, PA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code CCL

product code CCL

Other: 2
Total: 2

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.