DUOPROSS SYRINGES— 510(k) K042500

Substantially Equivalent

Duopross Meditech Corporation

FDA 510(k) clearance K042500 for DUOPROSS SYRINGES, Substantially Equivalent on 2005-02-22. Applicant: Duopross Meditech Corporation.

Clearance details

Applicant: Duopross Meditech Corporation
Product code: Code FMF
Advisory panel: General Hospital
Date received: 2004-09-14
Decision date: 2005-02-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Albuquerque, NM, US

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Adverse events under product code FMF

product code FMF

Death: 15
Injury: 2,263
Malfunction: 29,722
Other: 17
Total: 32,017

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.