K934385

Substantially Equivalent

MINIPACK 3100/3000 MODIFICATION

Applicant: Pace Tech, Inc.
Product code: DXN
Advisory panel: Cardiovascular
Date received: 1993-09-09
Decision date: 1994-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clearwater, FL, US

Adverse events under product code DXN

product code DXN

Death: 3
Injury: 169
Malfunction: 1,019
Other: 2
Total: 1,193

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.