VACUETTE MULTI-SAMPLE NEEDLE— 510(k) K973620

Substantially Equivalent

Greiner Meditech, Inc.

FDA 510(k) clearance K973620 for VACUETTE MULTI-SAMPLE NEEDLE, Substantially Equivalent on 1997-12-17. Applicant: Greiner Meditech, Inc..

Clearance details

Applicant: Greiner Meditech, Inc.
Product code: Code FMI
Advisory panel: General Hospital
Date received: 1997-09-23
Decision date: 1997-12-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bel Air, MD, US

Download summary PDF View on FDA.gov ↗

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.