cmAngio® (V1.6)
K-Number: K250754 · 2025-04-10
Device Summary
Frequently Asked Questions
What is the cmAngio® (V1.6)?
cmAngio® (V1.6) is a medical device that received FDA 510(k) clearance on 2025-04-10. The listed applicant is Curemetrix, Inc.. The 510(k) number is K250754.
When did cmAngio® (V1.6) receive FDA 510(k) clearance?
cmAngio® (V1.6) received FDA 510(k) clearance on 2025-04-10, under 510(k) number K250754.
Who is the listed applicant for cmAngio® (V1.6)?
The FDA 510(k) record lists Curemetrix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for cmAngio® (V1.6)?
The FDA product code for cmAngio® (V1.6) is QIH.
Other records listing Curemetrix, Inc. 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.