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#
- 8010298
- 8010482
- 3008264111
- 8043752
- 3045853999
- 3006154292
- 3001084743
- 3015512299
- 3002675176
- 8040263
- 3027187888
- 1416612
- 9680874
- 3004892425
- 3004598675
- 3003431869
- 3039414397
- 9616246
- 3013247477
- 9614093
- 3002858762
- 1720747
- 3008808049
- 1057946
- 3004168759
- 3012995405
- 3011600579
- 1123010
- 3003905396
- 3010262192
- 3001297506
- 3008770252
- 9610773
- 9610612
- 3003759558
- 3007648354
- 9611503
- 3003882387
- 9613926
- 3011371465
- 3001620590
- 1932180
- 2081040
- 3003877407
- 3009513193
- 9681540
- 8040278
- 3012541976
- 1926681
- 3004608878
- 3010687973
- 3013557562
- 3032747418
- 3035678069
- 3009255580
- 3003807268
- 3010288346
- 3010041511
- 3010707607
- 3026875454
- 3007597038
- 3010399422
- 3014334038
- 9613079
- 3011585752
- 3012226300
- 9680718
- 3036795921
- 9613910
- 3011301313
- 1313525
- 3005440795
- 1836161
- 3005528784
- 9613083
- 3013846070
- 1417592
- 9612278
- 3021680161
- 3010726901
Source Documents#
510(k) summary PDF not indicated by FDA