GLUCOSE REAGENT FOR BECKMAN SYNCHRON CX & CX DELTA SYSTEMS— 510(k) K033055

Substantially Equivalent

Diamond Diagnostics, Inc.

FDA 510(k) clearance K033055 for GLUCOSE REAGENT FOR BECKMAN SYNCHRON CX & CX DELTA SYSTEMS, Substantially Equivalent on 2004-01-30. Applicant: Diamond Diagnostics, Inc..

Clearance details

Applicant: Diamond Diagnostics, Inc.
Product code: Code CGA
Advisory panel: Clinical Chemistry
Date received: 2003-09-29
Decision date: 2004-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Holliston, MA, US

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Adverse events under product code CGA

product code CGA

Death: 2
Malfunction: 1,816
Total: 1,818

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.