DMA OXYGEN MONITOR— 510(k) K852823

Substantially Equivalent

Ferguson Medical

FDA 510(k) clearance K852823 for DMA OXYGEN MONITOR, Substantially Equivalent on 1985-10-29. Applicant: Ferguson Medical.

Clearance details

Applicant: Ferguson Medical
Product code: Code CCL
Advisory panel: Anesthesiology
Date received: 1985-07-01
Decision date: 1985-10-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chico, CA, 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.