Imbio Segmentation Editing Tool software
K-Number: K180129 · 2018-03-16
Device Summary
Frequently Asked Questions
What is the Imbio Segmentation Editing Tool software?
Imbio Segmentation Editing Tool software is a medical device that received FDA 510(k) clearance on 2018-03-16. The listed applicant is Imbio, LLC. The 510(k) number is K180129.
When did Imbio Segmentation Editing Tool software receive FDA 510(k) clearance?
Imbio Segmentation Editing Tool software received FDA 510(k) clearance on 2018-03-16, under 510(k) number K180129.
Who is the listed applicant for Imbio Segmentation Editing Tool software?
The FDA 510(k) record lists Imbio, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Imbio Segmentation Editing Tool software?
The FDA product code for Imbio Segmentation Editing Tool software is LLZ.
Other records listing Imbio, LLC 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: 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.