DeviceClearance

K935781

Unknown

ARGYLE SALEM SUMP TUBE ANTI-REFLUX VALVE INSERTION TRAY

Applicant
Sherwood Medical Co.
Product code
FEG
Advisory panel
Gastroenterology, Urology
Date received
Decision date
Decision
Unknown
Clearance type
Traditional
Location
St. Louis, MO, US
Download summary PDF View on FDA.gov ↗

Adverse events under product code FEG

product code FEG
Death
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.