510(k) K874966
- Device
- TUNING FORKS
- Applicant
- SOLWAY, INC.
- 510(k) number
- K874966
- Product code
- GWX
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1988-01-04
- Date received
- 1987-12-02
- 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#
- Contact
- MARTIN MUNZER
- Address
- Post Office Box 7647 Hollywood FL US 33081 33081
FDA Registration Numbers#
- 3023657851
- 9611112
- 3005440795
- 3004215117
- 2249529
- 9610617
- 1421879
- 3009703496
- 3004892425
- 8040278
- 3002090132
- 3010041511
- 3035678069
- 3016170451
- 3010687973
- 8010427
- 8040263
- 9681540
- 9611283
- 9613926
- 3007597038
- 3004598675
- 3010399422
- 3011585752
- 3003759558
- 1313525
- 3012541976
- 8043816
- 3010707607
- 3009255580
- 3008808049
- 9680874
- 9613910
- 3001297506
- 3027556548
- 3003771601
- 3002675176
- 3001620590
- 3004168759
- 8010704
- 8041151
- 1000426080
- 3004001706
- 9610773
- 1836161
- 3002858762
- 3010726901
- 3014908171
- 3029082594
- 3010288346
- 3012226300
- 8040884
- 9616246
- 9611503
- 3026875454
- 3003418325
- 3024088964
- 9614093
- 3013557562
- 2435946
- 3011137372
- 2081040
- 3010202439
- 3010353847
- 1417592
- 3010262192
- 3011499367
- 3013846070
- 9681622
- 1424478
- 2916714
- 3003431869
- 8010298
- 9613083
- 3007773213
- 1123010
- 1057946
- 3013784566
- 1416612
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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