K981619

Substantially Equivalent

VACUETTE MULTIPLE SAMPLE LUER ADAPTER

Applicant: Greiner Meditech, Inc.
Product code: FMI
Advisory panel: General Hospital
Date received: 1998-05-06
Decision date: 1998-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bel Air, MD, US

Adverse events under product code FMI

product code FMI

Death: 28
Injury: 1,517
Malfunction: 23,981
Other: 18
Total: 25,544

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.