510(k) K243060
- Device
- TeleRPM Gen2 Blood Glucose Monitoring System
- Applicant
- Guangdong Transtek Medical Electronics Co., Ltd.
- 510(k) number
- K243060
- Product code
- NBW
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2025-01-30
- Date received
- 2024-09-27
- Regulation
- 862.1345
- Classification name
- System, Test, Blood Glucose, Over The Counter
- Medical specialty
- Clinical Chemistry
- Review panel
- Clinical Chemistry
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- N
- Source
- FDA openFDA 510(k) dataset plus migrated FDA.report data
Related Records
Applicant Contact
- Contact
- Qian Mark
- Address
- Zone A, # 105, Dongli Rd., Torch Development District Zhongshan CN 528437 528437
FDA Registration Numbers
- 1450662
- 2030633
- 3012188053
- 3004009431
- 3030979885
- 1066444
- 3021286079
- 3013160357
- 3004145393
- 3022418645
- 3038419886
- 3005395953
- 3006371704
- 3007384659
- 3006733253
- 3015109923
- 3021611414
- 3022346573
- 1037998
- 3005862821
- 3016525500
- 9612841
- 3043013796
- 3011213605
- 3011979858
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- 3030311186
- 3006755541
- 3008780388
- 3012725363
- 3031789039
- 1616487
- 3004183148
- 3015997711
- 9616530
- 3003422726
- 3043025312
- 3010131137
- 3005706626
- 3008700497
- 3008514395
- 3003902721
- 3008789114
- 3013223546
- 3007031103
- 3003917514
- 3004167884
- 3022147580
- 3013298431
- 3030186688
- 9610126
- 3002807314
- 3043513123
- 3018940143
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- 3014302067
- 3009129531
- 3010713600
- 3012014399
- 3007421145
- 1649661
- 3005627859
- 3010564249
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- 2531491
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- 3011420269
- 3003366417
- 3001058982
- 3033530347
- 3013957847
- 3026260647
- 3011191255
- 3034603279
- 1000134386
- 1219029
- 3030978471
- 3005621222
- 3003741676
- 9710492
- 1000115322
- 3004539335
- 3013896610
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- 1832216
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- 1181121
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- 3012104670
- 1220477
- 3015188281
- 3007363438
- 3013472743
- 3007499349
- 3006532271
- 3011393376
- 3010830834
- 3015489159
- 3006537560
- 3002736372
- 2029275
- 3012133212
- 3020976354
- 3021841051
- 3004637226
- 3004101980
- 3032948391
- 3020460367
- 3008606429
- 3008573045
- 3004130086
- 3014353045
- 3042301847
- 3005393828
- 3024512705
- 3033394445
- 3042364147
- 3007134734
- 3007171717
- 3011065399
- 3017548799
- 3017550662
- 3012118659
- 9615507
- 1450743
- 3005798905
- 9611444
- 3009204541
- 1000113657
- 3014353121
- 3015967131
- 3017086896
- 3024379416
- 3008824097
- 3011536730
- 3001452053
- 3004193489
- 3020885868
- 3017500903
- 1832816
- 1810909
- 3010622184
- 3042026207
Source Documents
FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON
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