510(k) clearances

Ureterorenoscope System

Shenzhen HugeMed Medical Technical Development Co., Ltd. · Gastroenterology, Urology

K240374Substantially EquivalentTraditionalFGB
Open FDA's page for this record
Third party flag
N
City
Shenzhen
Advisory committee description
Gastroenterology, Urology
Address 1
401, 501, Bldg. 4, Haizhi Technology Park, Fortis, #17
Address 2
Bulan Rd.,Xialilang Community, Nanwan St., Longgang District
Statement or summary
Summary
Product code
FGB
Zip code
518115
Applicant
Shenzhen HugeMed Medical Technical Development Co., Ltd.
Decision date
2024-05-10
Decision code
SESE
Country code
CN
Device name
Ureterorenoscope System
Advisory committee
GU
Contact
Cathy Shi
K number
K240374
Date received
2024-02-07
Review advisory committee
GU
Postal code
518115
Decision description
Substantially Equivalent
Clearance type
Traditional
Harmonized identifiers (openFDA)
Device name
Ureteroscope And Accessories, Flexible/Rigid
Medical specialty description
Gastroenterology, Urology
Regulation number
876.1500
Device class
2
Registration number
3025349506, 3013247477, 8010047, 3042940358, 3029981244, 8010298, 1000484830, 3012322232, 3019807891, 2531475, 9616693, 3010707607, 9610773, 1418479, 3033010858, 3022106566, 3003782610, 3008439484, 3035484431, 3004111573, 3002808148, 9611612, 2936485, 9614434, 3011986317, 9610877, 3028058843, 3024021261, 3008998256, 1221826, 3020369549, 3011050570, 3003542872, 9610617, 1000121056, 3014683069, 3013992977, 1820334, 3010202439, 3037966040 +80 more
FEI number
3003448211, 3025349506, 3013247477, 3006149253, 3002806565, 3042940358, 3029981244, 3002808273, 1000484830, 3012322232, 3019807891, 3002807847, 3010707607, 3008185830, 1418479, 3033010858, 3022106566, 3003782610, 3008439484, 3035484431, 3004111573, 3002808148, 3000206435, 3002808268, 2936485, 4430, 3011986317, 1000138054, 3028058843, 3024021261, 3002806359, 3008998256, 1221826, 3020369549, 3011050570, 3003542872, 1000121056, 3014683069, 3013992977, 1820334 +80 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.