DeviceClearance

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. Device class: 2.

Clearance details

Applicant
Ferguson Medical
Product code
Code CCL
Device class
Class 2
Regulation
21 CFR 868.1720
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Chico, CA, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code CCL

product code CCL
Other
2
Total
2

Source: openFDA MAUDE database, through . 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.