510(k) clearances

PV-iCurve Pro

Perception Vision Medical Technology Co., Ltd. · Radiology

K261531Substantially EquivalentTraditionalLLZ
Open FDA's page for this record
Third party flag
N
City
Guangzhou
Advisory committee description
Radiology
Address 1
Rm. 1305, 1306, 1307, 1311, Block B, Zhongda Science And Tec
Address 2
Bldg. 705, W. District, Yard Garden, # 135, Xingang W. Rd.,
Statement or summary
Summary
Product code
LLZ
Applicant
Perception Vision Medical Technology Co., Ltd.
Decision date
2026-10-21
Decision code
SESE
Country code
CN
Device name
PV-iCurve Pro
Advisory committee
RA
Contact
Xuling Lu
K number
K261531
Date received
2026-05-08
Review advisory committee
RA
Decision description
Substantially Equivalent
Clearance type
Traditional
Harmonized identifiers (openFDA)
Device name
System, Image Processing, Radiological
Medical specialty description
Radiology
Regulation number
892.2050
Device class
2
Registration number
3001052305, 3005406110, 3017545364, 3005172103, 9617978, 3004706313, 3008487708, 1226544, 3009341091, 3044776706, 3010656400, 3038189169, 3007362683, 3007993775, 1061158, 3014232555, 3003757027, 3014991167, 9617592, 3013634985, 3023217364, 1054415, 3013535906, 3026047529, 3019878658, 3005225421, 3030655434, 3009156722, 3010445368, 8020825, 3011676026, 3008364043, 3045521711, 3014635169, 2954921, 9615439, 3011015597, 3003989064, 3035371452, 3019544554 +603 more
FEI number
3001052305, 3005406110, 3017545364, 3005172103, 3004706313, 3008487708, 3009341091, 3044776706, 3002808188, 3010656400, 3038189169, 3007362683, 3007993775, 3014232555, 3003757027, 3014991167, 3013634985, 3023217364, 3013535906, 3026047529, 3019878658, 3005225421, 3030655434, 3009156722, 3010445368, 3011676026, 3008364043, 3045521711, 3014635169, 3011015597, 3003989064, 3035371452, 3019544554, 3008548323, 3014269683, 3002821504, 2126677, 3002619595, 3010684280, 3003861317 +603 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.