510(k) K813304
- Device
- CONPHAR, TUNING FORKS
- Applicant
- CONPHAR, INC.
- 510(k) number
- K813304
- Product code
- GWX
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1981-12-10
- Date received
- 1981-11-23
- Regulation
- 882.1525
- Classification name
- Fork, Tuning
- Medical specialty
- Neurology
- Review panel
- Neurology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 1057946
- 3010262192
- 3010041511
- 3010687973
- 3027556548
- 9611112
- 2020550
- 9680874
- 3006154292
- 9680718
- 1720747
- 3036795921
- 3002807115
- 3039414397
- 3003807268
- 3010202439
- 9680518
- 3011585752
- 9612074
- 3011497622
- 9613083
- 1421879
- 3001084743
- 3012226300
- 9610617
- 9610905
- 3003905396
- 3021680161
- 3003418325
- 3003431869
- 8043816
- 8030607
- 3004168759
- 8010482
- 3007648354
- 3011600579
- 1313525
- 9680002
- 2249529
- 3009703496
- 3026875454
- 3010707607
- 8010427
- 8010298
- 3005067367
- 3005809810
- 1932180
- 3003771601
- 3012541976
- 3010726901
- 9611283
- 3015069921
- 1123010
- 3004215117
- 3003782614
- 3032747418
- 8040278
- 9613910
- 9616246
- 3001297506
- 1424478
- 9610612
- 3014334038
- 3002858762
- 9612278
- 3008808049
- 3013247477
- 3011499367
- 3015512299
- 9681622
- 3014908171
- 8040884
- 1926681
- 3007773213
- 3007597038
- 3011137372
- 3001620590
- 2432177
- 3003759558
- 3010288346
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code GWX #
Legacy Summary#
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FDA Review#
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