510(K) CLEARANCES 49 ▼18RECALLS POSTED 23 ▼3CLASS I 1 ▼1PMA DECISIONS 37 ▼3WEEK ENDING / FDA DATA AS OF
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K132341Substantially Equivalent

Dc-8/ Dc-8 Pro/ Dc-8 Cv/ Dc-8 Exp/ Dc-8S Diagnostic Ultrasound Systems

Shenzhen Mindray Bio-Medical Electronics Co.,LTD, Nanshan, Shenzhen, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K132341 is the FDA 510(k) clearance record for DC-8/ DC-8 PRO/ DC-8 CV/ DC-8 EXP/ DC-8S DIAGNOSTIC ULTRASOUND SYSTEMS, a class II device, cleared for Shenzhen Mindray Bio-Medical Electronics Co., Ltd. on under FDA product code IYN (System, Imaging, Pulsed Doppler, Ultrasonic). FDA records list 160 510(k) clearances for Shenzhen Mindray Bio-Medical Electronics Co., Ltd., from to . As of , FDA records show no recalls naming K132341.

Clearance record

Decision date
Received
(20 days to decision)
Product code
IYN System, Imaging, Pulsed Doppler, Ultrasonic
Regulation
21 CFR 892.1550
Device class
Class II
Review panel
Radiology
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd. Mindray Bldg.,Keji 12th Rd. S.,, Nanshan, Shenzhen, CN
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code IYN

Trailing 12 months
56 clearances under product code IYN in the twelve months to October 2026, May 2026 the highest month at 11.
Show the numbers
Monthly 510(k) clearances under FDA product code IYN, trailing twelve months
MonthClearances
November 20256
December 20256
January 20264
February 20261
March 20266
April 20263
May 202611
June 20263
July 20266
August 20263
September 20263
October 20264