510(k) K801468
- Device
- FRAZIER-FERGUSON SUCTION TUBES
- Applicant
- EDWARD WECK, INC.
- 510(k) number
- K801468
- Product code
- KCB
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1980-08-12
- Date received
- 1980-06-24
- Regulation
- 874.4420
- Classification name
- Tube, Tonsil Suction
- Medical specialty
- Ear Nose & Throat
- Review panel
- Ear Nose & Throat
- 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#
- 3005071827
- 1057946
- 3011625373
- 3010041511
- 3027556548
- 3043239665
- 3003644849
- 3005061536
- 3036795921
- 3039414397
- 9613083
- 1421879
- 3004571672
- 3010455030
- 3012226300
- 3011258423
- 9611367
- 9610905
- 8010273
- 9710524
- 9710058
- 3003905396
- 3021680161
- 3003418325
- 3003431869
- 3015895045
- 8030607
- 3013946322
- 3003761012
- 3011600579
- 1313525
- 9680002
- 3008280196
- 8010372
- 3010699884
- 3005067367
- 9680837
- 1932180
- 3003965134
- 9611283
- 3007507973
- 3005813597
- 3012507533
- 3004215117
- 1032227
- 8010159
- 8040233
- 3032747418
- 8040278
- 3001297506
- 1056350
- 3008808049
- 3011499367
- 3045058049
- 3010829427
- 3002834291
- 3015512299
- 3013497507
- 9681622
- 2431166
- 8040884
- 9611102
- 3007773213
- 1052728
- 3011137372
- 3017953405
- 8010733
- 3005528784
- 3004598675
- 3006487092
- 3003032798
- 3034669683
- 1836161
- 2080222
- 3002675176
- 3004608878
- 9680515
- 9614986
- 8040881
- 3015351976
Source Documents#
510(k) summary PDF not indicated by FDA
Legacy Summary#
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FDA Review#
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