510(k) K243613
- Device
- Patch-TEA (Model TRI-21)
- Applicant
- Transtimulation Research, Inc.
- 510(k) number
- K243613
- Product code
- NUH
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2025-04-09
- Date received
- 2024-11-22
- Regulation
- 882.5890
- Classification name
- Stimulator, Nerve, Transcutaneous, Over-The-Counter
- Medical specialty
- Neurology
- Review panel
- Neurology
- 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
- Victor Pikov
- Address
- 800 Research Pkwy., # 337 Oklahoma City OK US 73104 73104
FDA Registration Numbers
- 3003895865
- 3014774380
- 3011050674
- 3004146401
- 3010402752
- 3004264602
- 3008585473
- 1528161
- 3012651177
- 3008729899
- 3033881629
- 3026164517
- 3012176966
- 3010162782
- 3030597665
- 8040537
- 3011564440
- 3008929787
- 3011120089
- 3012386142
- 3012446970
- 3017450375
- 3007731000
- 3043013796
- 3027241812
- 3026264
- 2023152
- 3010485091
- 2000004234
- 3012725363
- 3012729332
- 3009437400
- 3017264244
- 1450057
- 3011267903
- 3017887847
- 3003740945
- 3030539046
- 3007543044
- 8030245
- 3010405397
- 3005170249
- 3006367638
- 3015142815
- 3009488655
- 3003255790
- 3018940143
- 3016452327
- 3014344342
- 3019822804
- 3005569927
- 3012316249
- 3002669614
- 2013558
- 3030412027
- 3030220267
- 3033847811
- 3007710601
- 3014601569
- 3038195193
- 3028172072
- 3012500350
- 3023237645
- 3023339107
- 3018514222
- 3021422553
- 1832894
- 3032062344
- 3007719656
- 3008973759
- 3033530347
- 3013957847
- 3038295706
- 9615033
- 3004541594
- 3011191255
- 2939821
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- 3003741676
- 3027062656
- 3010417025
- 3004839404
- 1055808
- 1063974
- 3006469120
- 3013865802
- 3011562129
- 3009888740
- 3023330992
- 3042268484
- 3008806536
- 3010852191
- 3011767724
- 3029924973
- 3015007456
- 3010078417
- 3023613474
- 3017953405
- 3006850006
- 3003446042
- 3006551156
- 3006626283
- 3007092044
- 3031464228
- 9616877
- 3020769982
- 3012840029
- 3025367760
- 3010770433
- 3007615436
- 3015619973
- 3008507279
- 3022929665
- 3015214304
- 3026322014
- 3016508547
- 3014314933
- 3017887928
- 3001373226
- 3011077581
- 3008011951
- 3037609256
- 3008573045
- 3005621440
- 3025428426
- 3039394880
- 3014647250
- 9616086
- 3001224205
- 3025235024
- 3038311114
- 3008048783
- 3026753375
- 3042190125
- 3011721071
- 3018109879
- 2024292
- 3010097863
- 8022077
- 3011412151
- 3015588280
- 3022631685
- 3029939996
- 3010894709
- 3007689716
- 3009494725
- 3010880718
- 9617486
- 2248223
- 3004049909
- 3030531253
- 3008770252
- 3016856381
- 3006852037
- 3009411292
- 9611558
- 2249769
Source Documents
FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON
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