DeviceClearance

K052083

Substantially Equivalent

NAVISTAR RMT STEERABLE TIP DIAGNOSTIC CATHETER

Applicant
Biosense Webster, Inc.
Product code
DRF
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Diamond Bar, CA, US
Download summary PDF View on FDA.gov ↗

Adverse events under product code DRF

product code DRF
Death
127
Injury
1,676
Malfunction
2,003
Other
1
Total
3,807

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.