K913751

Substantially Equivalent

PRESSURE INFUSER

Applicant: Biomedical Dynamics, Inc.
Product code: KZD
Advisory panel: General Hospital
Date received: 1991-08-21
Decision date: 1992-01-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burnsville, MN, US

Adverse events under product code KZD

product code KZD

Death: 4
Total: 4

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.