cmAngio® V1.0
K-Number: K232367 · 2023-10-05
Device Summary
Frequently Asked Questions
What is the cmAngio® V1.0?
cmAngio® V1.0 is a medical device that received FDA 510(k) clearance on 2023-10-05. The listed applicant is Curemetrix, Inc.. The 510(k) number is K232367.
When did cmAngio® V1.0 receive FDA 510(k) clearance?
cmAngio® V1.0 received FDA 510(k) clearance on 2023-10-05, under 510(k) number K232367.
Who is the listed applicant for cmAngio® V1.0?
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® V1.0?
The FDA product code for cmAngio® V1.0 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.