SmartTouch
K-Number: K173310 · 2018-03-26
Device Summary
Frequently Asked Questions
What is the SmartTouch?
SmartTouch is a medical device that received FDA 510(k) clearance on 2018-03-26. The listed applicant is Adherium (Nz), Ltd.. The 510(k) number is K173310.
When did SmartTouch receive FDA 510(k) clearance?
SmartTouch received FDA 510(k) clearance on 2018-03-26, under 510(k) number K173310.
Who is the listed applicant for SmartTouch?
The FDA 510(k) record lists Adherium (Nz), Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SmartTouch?
The FDA product code for SmartTouch is CAF.
Other records listing Adherium (Nz), 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: CAF)
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.