CMS600P2 B-Ultrasound Diagnostic System
K-Number: K170856 · 2017-11-17
Device Summary
Frequently Asked Questions
What is the CMS600P2 B-Ultrasound Diagnostic System?
CMS600P2 B-Ultrasound Diagnostic System is a medical device that received FDA 510(k) clearance on 2017-11-17. The listed applicant is Contec Medical Systems Co.,Ltd. The 510(k) number is K170856.
When did CMS600P2 B-Ultrasound Diagnostic System receive FDA 510(k) clearance?
CMS600P2 B-Ultrasound Diagnostic System received FDA 510(k) clearance on 2017-11-17, under 510(k) number K170856.
Who is the listed applicant for CMS600P2 B-Ultrasound Diagnostic System?
The FDA 510(k) record lists Contec Medical Systems Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CMS600P2 B-Ultrasound Diagnostic System?
The FDA product code for CMS600P2 B-Ultrasound Diagnostic System is IYO.
Other records listing Contec Medical Systems 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: IYO)
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.