DeviceClearance

K802883

Substantially Equivalent

T3-SQUIBB RIA KIT

Applicant
E. R. Squibb & Sons, Inc.
Product code
CDP
Advisory panel
Clinical Chemistry
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
New Brunswick, NJ, US
Download summary PDF View on FDA.gov ↗

Adverse events under product code CDP

product code CDP
Malfunction
647
Total
647

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.