Ventripoint Medical System Plus (VMS+) 4.0
K-Number: K241222 · 2025-02-26
Device Summary
Frequently Asked Questions
What is the Ventripoint Medical System Plus (VMS+) 4.0?
Ventripoint Medical System Plus (VMS+) 4.0 is a medical device that received FDA 510(k) clearance on 2025-02-26. The listed applicant is Ventripoint Diagnostics , Ltd.. The 510(k) number is K241222.
When did Ventripoint Medical System Plus (VMS+) 4.0 receive FDA 510(k) clearance?
Ventripoint Medical System Plus (VMS+) 4.0 received FDA 510(k) clearance on 2025-02-26, under 510(k) number K241222.
Who is the listed applicant for Ventripoint Medical System Plus (VMS+) 4.0?
The FDA 510(k) record lists Ventripoint Diagnostics , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ventripoint Medical System Plus (VMS+) 4.0?
The FDA product code for Ventripoint Medical System Plus (VMS+) 4.0 is QIH.
Other records listing Ventripoint Diagnostics , Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: QIH)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.