BAROSENSE ENDOGASTRIC TUBE AND INTRODUCER BOUGIE— 510(k) K120126

Substantially Equivalent

Barosense, Inc.

FDA 510(k) clearance K120126 for BAROSENSE ENDOGASTRIC TUBE AND INTRODUCER BOUGIE, Substantially Equivalent on 2012-09-10. Applicant: Barosense, Inc..

Clearance details

Applicant: Barosense, Inc.
Product code: Code FED
Advisory panel: Gastroenterology, Urology
Date received: 2012-01-17
Decision date: 2012-09-10
Decision: Substantially Equivalent
Clearance type: Special
Location: Redwood City, CA, US

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Adverse events under product code FED

product code FED

Death: 10
Total: 10

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.