MODEL 2331T PATIENT PROGRAMMER— 510(k) K880738

Substantially Equivalent

Medtronic Vascular

FDA 510(k) clearance K880738 for MODEL 2331T PATIENT PROGRAMMER, Substantially Equivalent on 1988-11-17. Applicant: Medtronic Vascular.

Clearance details

Applicant: Medtronic Vascular
Product code: Code KRG
Advisory panel: Cardiovascular
Date received: 1988-02-24
Decision date: 1988-11-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KRG

product code KRG

Malfunction: 8,377
Total: 8,377

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.