DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System
K-Number: K173369 · 2017-12-13
Decision Date2017-12-13
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System is a medical device manufactured by Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd.. It received FDA 510(k) clearance on 2017-12-13 under approval number K173369. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd.. The 510(k) number is K173369.
When was DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System approved by the FDA?
DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System received FDA 510(k) clearance on 2017-12-13, under approval number K173369.
What company makes 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 manufactured by Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd..
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.
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Other Devices by Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd.
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K202785Resona R9,Resona R9 Exp,Resona R9 Pro,Resona R9S, Nuewa R9,Nuewa R9 Exp,Nuewa R9 Pro,Nuewa R9S,Resona 7,Resona 7CV,Resona 7EXP,Resona 7S, Resona 7OB,Resona 7PRO,Imagyn 7,Resona Y Diagnostic Ultrasound System
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Related Devices (Code: IYN)
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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.