IT-III active System
K-Number: K181137 · 2018-11-16
Device Summary
Frequently Asked Questions
What is the IT-III active System?
IT-III active System is a medical device that received FDA 510(k) clearance on 2018-11-16. The listed applicant is Neobiotech Co., Ltd.. The 510(k) number is K181137.
When did IT-III active System receive FDA 510(k) clearance?
IT-III active System received FDA 510(k) clearance on 2018-11-16, under 510(k) number K181137.
Who is the listed applicant for IT-III active System?
The FDA 510(k) record lists Neobiotech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IT-III active System?
The FDA product code for IT-III active System is DZE.
Other records listing Neobiotech Co., 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: DZE)
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.