Ventripoint Diagnostics , Ltd.

Ventripoint Diagnostics , Ltd. holds 3 FDA 510(k) medical device clearances, first cleared 2018, most recent 2025.

Top product codes for Ventripoint Diagnostics , Ltd.

Recent clearances by Ventripoint Diagnostics , Ltd.

K241222 — Ventripoint Medical System Plus (VMS+) 4.0Code QIH·2025-02-26
K191493 — Ventripoint Medical System Plus (VMS+) 3.0Code LLZ·2019-10-16
K173810 — Ventripoint Medical System Plus (VMS+)Code IYN·2018-05-14

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