P60 Series Digital Color Doppler Ultrasound System

System, Imaging, Pulsed Doppler, Ultrasonic

SONOSCAPE MEDICAL CORP.

The following data is part of a premarket notification filed by Sonoscape Medical Corp. with the FDA for P60 Series Digital Color Doppler Ultrasound System.

Pre-market Notification Details

Device IDK171000
510k NumberK171000
Device Name:P60 Series Digital Color Doppler Ultrasound System
ClassificationSystem, Imaging, Pulsed Doppler, Ultrasonic
Applicant SONOSCAPE MEDICAL CORP. 4/F, 5/F, 8/F, 9/F & 10/F, Yizhe Building, Yuquan Road, Nanshan Shenzhen,  CN 518051
ContactToki Wu
CorrespondentToki Wu
SONOSCAPE MEDICAL CORP. 4/F, 5/F, 8/F, 9/F & 10/F, Yizhe Building, Yuquan Road, Nanshan Shenzhen,  CN 518051
Product CodeIYN  
Subsequent Product CodeITX
Subsequent Product CodeIYO
CFR Regulation Number892.1550 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2017-04-03
Decision Date2017-07-11
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
06945868616052 K171000 000
B369MUS05220 K171000 000
B369MUS05219 K171000 000
B369MUS05218 K171000 000
B369MUS05217 K171000 000
B369MUS05216 K171000 000
B369MUS05215 K171000 000
B369MUS05214 K171000 000
B369MUS05213 K171000 000
B369MUS05212 K171000 000
B369MUS05211 K171000 000
B369MUS05210 K171000 000
B369MUS05209 K171000 000
B369MUS05208 K171000 000
B369MUS05203 K171000 000
B369MUS05221 K171000 000
B369MUS05222 K171000 000
B369MUS05223 K171000 000
06945868616045 K171000 000
06945868616038 K171000 000
06945868616021 K171000 000
B369MUS05235 K171000 000
B369MUS05234 K171000 000
B369MUS05233 K171000 000
B369MUS05231 K171000 000
B369MUS05230 K171000 000
B369MUS05229 K171000 000
B369MUS05228 K171000 000
B369MUS05227 K171000 000
B369MUS05226 K171000 000
B369MUS05225 K171000 000
B369MUS05224 K171000 000
B369MUS01030 K171000 000

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.