510(k) clearances

Diagnostic Ultrasound System (Nuewa A20W); Diagnostic Ultrasound System (Nuewa A20); Diagnostic Ultrasound System (Nuewa A20 Exp); Diagnostic Ultrasound System (Nuewa A20 Elite); Diagnostic Ultrasound System (Nuewa A20Q); Diagnostic Ultrasound System (Nuewa A MV); Diagnostic Ultrasound System (Nuewa A Elite); Diagnostic Ultrasound System (Nuewa A MS); Diagnostic Ultrasound System (Nuewa A20 Premium); Diagnostic Ultrasound System (Nuewa A20 Plus); Diagnostic Ultrasound System (Nuewa A18

Shenzhen Mindray Bio-Medical Electronics Co., Ltd. · Radiology

K261585Substantially EquivalentTraditionalIYN
Open FDA's page for this record
Third party flag
N
City
Shenzhen
Advisory committee description
Radiology
Address 1
Mindray Bldg., Keji 12th Rd. S., Hi-Tech Industrial Park, Na
Statement or summary
Summary
Product code
IYN
Zip code
518057
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Decision date
2026-10-16
Decision code
SESE
Country code
CN
Advisory committee
RA
Contact
Xiaolong Fan
K number
K261585
Date received
2026-05-13
Review advisory committee
RA
Postal code
518057
Decision description
Substantially Equivalent
Clearance type
Traditional
Device name

Diagnostic Ultrasound System (Nuewa A20W); Diagnostic Ultrasound System (Nuewa A20); Diagnostic Ultrasound System (Nuewa A20 Exp); Diagnostic Ultrasound System (Nuewa A20 Elite); Diagnostic Ultrasound System (Nuewa A20Q); Diagnostic Ultrasound System (Nuewa A MV); Diagnostic Ultrasound System (Nuewa A Elite); Diagnostic Ultrasound System (Nuewa A MS); Diagnostic Ultrasound System (Nuewa A20 Premium); Diagnostic Ultrasound System (Nuewa A20 Plus); Diagnostic Ultrasound System (Nuewa A18

Harmonized identifiers (openFDA)
Device name
System, Imaging, Pulsed Doppler, Ultrasonic
Medical specialty description
Radiology
Regulation number
892.1550
Device class
2
Registration number
1000602763, 3005403518, 3003600763, 3005406110, 3018094310, 9710090, 3003774756, 1062741, 3008487708, 3008729547, 1000513161, 2518897, 3014555455, 8010047, 3010703925, 3003589956, 3017955833, 9616774, 3009499478, 9680269, 3003899230, 3010663777, 2521877, 3010398867, 3003681187, 3005334138, 3003637092, 3011686611, 3016436764, 1054713, 2134812, 3016493665, 3010390468, 3026047529, 3003412859, 3002808148, 3009196578, 3015806723, 3011137372, 3009156722 +182 more
FEI number
1000602763, 3005403518, 3003600763, 3005406110, 3018094310, 3003774756, 3008487708, 3008729547, 1000513161, 3014555455, 3010703925, 3003309342, 3003589956, 3017955833, 3003408255, 3009499478, 3002808127, 3003899230, 1000124215, 3010663777, 2521877, 3010398867, 3003681187, 3005334138, 3003637092, 3011686611, 3002808529, 3016436764, 3002808382, 3016493665, 3010390468, 3026047529, 3003412859, 3000957797, 3002808148, 3009196578, 3015806723, 3009156722, 3027501622, 3019216 +182 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.