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#
- 3026875454
- 3007597038
- 3021680161
- 3005528784
- 3004168759
- 9610905
- 3003882387
- 3036795921
- 3001297506
- 3011371465
- 3003905396
- 3016170451
- 8010482
- 3005440795
- 3001084743
- 3015512299
- 3039414397
- 3004608878
- 3014342096
- 3007648354
- 3010726901
- 3012995405
- 9611112
- 9613083
- 3005809810
- 3012226300
- 9613910
- 3045853999
- 9610612
- 3015069921
- 8010298
- 3003431869
- 3008264111
- 9680002
- 8030607
- 2434008
- 3001620590
- 1000426080
- 3008808049
- 3004598675
- 3011137372
- 2432177
- 3003407244
- 3003759558
- 1932180
- 1926681
- 3005067367
- 3004892425
- 9614093
- 3010399422
- 8043816
- 3007773213
- 8040263
- 8040884
- 3027187888
- 3004001706
- 3029082594
- 3010041511
- 8041151
- 3009255580
- 2249529
- 9610773
- 3002090132
- 3010353847
- 3002858762
- 3004215117
- 1720747
- 8043752
- 3014908171
- 2081040
- 9612278
- 3003877407
- 1123010
- 3013784566
- 1424478
- 3013846070
- 1421101
- 3011499367
- 3002807115
- 3032747418
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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