Pinpoint GT Needle Guide Kits— 510(k) K171348

Substantially Equivalent

C.R. Bard, Inc.

FDA 510(k) clearance K171348 for Pinpoint GT Needle Guide Kits, Substantially Equivalent on 2017-05-22. Applicant: C.R. Bard, Inc..

Clearance details

Applicant: C.R. Bard, Inc.
Product code: Code ITX
Advisory panel: Radiology
Date received: 2017-05-08
Decision date: 2017-05-22
Decision: Substantially Equivalent
Clearance type: Special
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code ITX

product code ITX

Death: 6
Injury: 137
Malfunction: 2,036
Total: 2,179

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.