IntelliCart System
K-Number: K172481 · 2017-09-14
Device Summary
Frequently Asked Questions
What is the IntelliCart System?
IntelliCart System is a medical device that received FDA 510(k) clearance on 2017-09-14. The listed applicant is Dornoch Medical Systems. The 510(k) number is K172481.
When did IntelliCart System receive FDA 510(k) clearance?
IntelliCart System received FDA 510(k) clearance on 2017-09-14, under 510(k) number K172481.
Who is the listed applicant for IntelliCart System?
The FDA 510(k) record lists Dornoch Medical Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IntelliCart System?
The FDA product code for IntelliCart System is JCX.
Other records listing Dornoch Medical Systems 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: JCX)
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.