DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System
K-Number: K173369 · 2017-12-13
Device Summary
Frequently Asked Questions
What is the DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System?
DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2017-12-13. The listed applicant is Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd.. The 510(k) number is K173369.
When did DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System receive FDA 510(k) clearance?
DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System received FDA 510(k) clearance on 2017-12-13, under 510(k) number K173369.
Who is the listed applicant for DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System?
The FDA 510(k) record lists Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System?
The FDA product code for DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System is IYN.
Other records listing Shenzhen Mindray Bio-Meidcal Electronics 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: IYN)
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.