SMARTFLOW— 510(k) K012947

Substantially Equivalent

Florence Medical , Ltd.

FDA 510(k) clearance K012947 for SMARTFLOW, Substantially Equivalent on 2001-10-02. Applicant: Florence Medical , Ltd..

Clearance details

Applicant: Florence Medical , Ltd.
Product code: Code DQK
Advisory panel: Cardiovascular
Date received: 2001-09-04
Decision date: 2001-10-02
Decision: Substantially Equivalent
Clearance type: Special
Location: Ra'Ananna 43373, IL

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Adverse events under product code DQK

product code DQK

Death: 10
Injury: 225
Malfunction: 2,123
Other: 2
Total: 2,360

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.