ImageGrid StreamVue
K-Number: K262143 · 2026-07-23
Device Summary
Frequently Asked Questions
What is the ImageGrid StreamVue?
ImageGrid StreamVue is a medical device that received FDA 510(k) clearance on 2026-07-23. The listed applicant is Candelis, Inc.. The 510(k) number is K262143.
When did ImageGrid StreamVue receive FDA 510(k) clearance?
ImageGrid StreamVue received FDA 510(k) clearance on 2026-07-23, under 510(k) number K262143.
Who is the listed applicant for ImageGrid StreamVue?
The FDA 510(k) record lists Candelis, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ImageGrid StreamVue?
The FDA product code for ImageGrid StreamVue is LLZ.
Related Devices (Code: LLZ)
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.