KSI

GAMMA ARACHIS HYPOGEA LECTIN

Advisory panel: Hematology
Total cleared: 4

Adverse events under product code KSI

product code KSI

Malfunction: 700
Total: 700

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 →

Recent clearances under product code KSI

K820368 — LECTIN-A American Dade · 1982-04-14
K813413 — LECTIN H American Dade · 1982-03-04
K792582 — POLY-LEC SYSTEM Gamma Biologicals, Inc. · 1980-01-16
K792583 — GAMMA ARACHIS HYPOGEA LECTIN Gamma Biologicals, Inc. · 1980-01-16

Data sourced from openFDA. This site is unofficial and independent of the FDA.