HYPODERMIC NEEDLES, SINGLE LUMEN— 510(k) K911397

Substantially Equivalent

Popper & Sons, Inc.

FDA 510(k) clearance K911397 for HYPODERMIC NEEDLES, SINGLE LUMEN, Substantially Equivalent on 1991-05-20. Applicant: Popper & Sons, Inc..

Clearance details

Applicant: Popper & Sons, Inc.
Product code: Code FCG
Advisory panel: Gastroenterology, Urology
Date received: 1991-03-29
Decision date: 1991-05-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Hyde Park, NY, US

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Adverse events under product code FCG

product code FCG

Death: 13
Injury: 576
Malfunction: 1,966
Total: 2,555

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.