MEDIGARD BLOOD COLLECTION DEVICE— 510(k) K082511

Substantially Equivalent

Medigard Limited

FDA 510(k) clearance K082511 for MEDIGARD BLOOD COLLECTION DEVICE, Substantially Equivalent on 2009-01-16. Applicant: Medigard Limited.

Clearance details

Applicant: Medigard Limited
Product code: Code FMI
Advisory panel: General Hospital
Date received: 2008-08-29
Decision date: 2009-01-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Crofton, MD, US

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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.