510(k) K760303
- Device
- Fork, Tuning Bk-7519
- Applicant
- FRED SAMMONS, INC.
- 510(k) number
- K760303
- Product code
- GWX
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1976-09-08
- Date received
- 1976-07-23
- 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#
- 9613083
- 3005440795
- 9611503
- 9611112
- 3010707607
- 3012995405
- 3013846070
- 3001297506
- 1057946
- 2432177
- 1000426080
- 3003782614
- 3003882387
- 1926681
- 3004168759
- 3010399422
- 3004215117
- 2081040
- 3014908171
- 3012541976
- 3005528784
- 3002807120
- 3035678069
- 8040263
- 1416612
- 3003418325
- 3004892425
- 9614093
- 3002090132
- 3008808049
- 8030607
- 9612278
- 9680874
- 3007597038
- 3010353847
- 9610617
- 3011585752
- 9680002
- 3021680161
- 3003877407
- 3013247477
- 3012226300
- 3003905396
- 9610905
- 3011301313
- 1421879
- 3002858762
- 3002675176
- 3027556548
- 3024088964
- 3014334038
- 9613926
- 2916714
- 3009513193
- 8043752
- 3011137372
- 9680718
- 3011371465
- 8010482
- 3010726901
- 3005067367
- 3009255580
- 3011499367
- 1932180
- 9610773
- 1836161
- 1417592
- 3004608878
- 1424478
- 9680518
- 9613079
- 1313525
- 8040278
- 3003807268
- 3007773213
- 3023657851
- 3001084743
- 3010202439
- 9611283
- 1720747
Source Documents#
510(k) summary PDF not indicated by FDA