NO-POKES NEEDLE SAFETY DEVICE— 510(k) K020921

Substantially Equivalent

Bemis Mfg. Co.

FDA 510(k) clearance K020921 for NO-POKES NEEDLE SAFETY DEVICE, Substantially Equivalent on 2002-07-11. Applicant: Bemis Mfg. Co..

Clearance details

Applicant: Bemis Mfg. Co.
Product code: Code FMI
Advisory panel: General Hospital
Date received: 2002-03-21
Decision date: 2002-07-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sheboygan Falls, WI, 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.