HYPODERMIC NEEDLE-PRO INSULIN SYRINE & NEEDLE WITH NEEDLE PROTECTION DEVICE— 510(k) K014073

Substantially Equivalent

Portex, Inc.

FDA 510(k) clearance K014073 for HYPODERMIC NEEDLE-PRO INSULIN SYRINE & NEEDLE WITH NEEDLE PROTECTION DEVICE, Substantially Equivalent on 2002-02-13. Applicant: Portex, Inc..

Clearance details

Applicant: Portex, Inc.
Product code: Code FMF
Advisory panel: General Hospital
Date received: 2001-12-10
Decision date: 2002-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Keene, NH, 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.