DeviceClearance

VENTREX OXYGEN SENSOR— 510(k) K963415

Substantially Equivalent

Ventrex, LLC

FDA 510(k) clearance K963415 for VENTREX OXYGEN SENSOR, Substantially Equivalent on 1996-11-25. Applicant: Ventrex, LLC.

Clearance details

Applicant
Ventrex, LLC
Product code
Code CCL
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Horsham, PA, US
Download summary PDFView on FDA.gov ↗

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.