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#
- 3039414397
- 3008808049
- 3003882387
- 3013247477
- 9681540
- 3005809810
- 2432177
- 2020550
- 8010427
- 9613079
- 3011137372
- 1416612
- 3010707607
- 3009703496
- 2081040
- 3010202439
- 3004168759
- 3002675176
- 2434008
- 3003431869
- 9611112
- 3002807115
- 3008264111
- 3011499367
- 9610617
- 3001620590
- 3010726901
- 9610773
- 3027187888
- 3009513193
- 3023657851
- 1417592
- 3010288346
- 3035678069
- 3002858762
- 3011585752
- 2435946
- 1720747
- 3003771601
- 3021680161
- 9680874
- 3011301313
- 3015512299
- 3002090132
- 3007773213
- 9681622
- 3013557562
- 9611283
- 9613910
- 3003782614
- 3004215117
- 3010041511
- 8040278
- 3011497622
- 3029082594
- 9614093
- 3024088964
- 3001084743
- 3010262192
- 8041151
- 1836161
- 9610905
- 8040263
- 2916714
- 9613083
- 9680518
- 3026875454
- 3015069921
- 3036795921
- 9616246
- 3006154292
- 1421879
- 3016170451
- 3004892425
- 1932180
- 1000426080
- 3003877407
- 1421101
- 1424478
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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