510(k) K822010
- Device
- RIGID SUCTION TIPS & RELATED ITEMS
- Applicant
- KELLEHER CORP.
- 510(k) number
- K822010
- Product code
- JZF
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1982-08-12
- Date received
- 1982-07-08
- Regulation
- 874.4420
- Classification name
- Tube, Ear 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#
- 3003965134
- 3018094310
- 3010288346
- 3026848699
- 1720747
- 1057421
- 8039051
- 3024988980
- 8043965
- 9612074
- 3007507973
- 3013503739
- 9611610
- 3010726901
- 3032747418
- 2084346
- 3011600579
- 3011137372
- 1313525
- 3009703496
- 8040278
- 1932214
- 9613073
- 3003761012
- 9614084
- 3008936260
- 1058020
- 8010433
- 3009255580
- 3008044484
- 9612501
- 3007064566
- 3007137643
- 3006142527
- 3011050570
- 1417592
- 9680718
- 8040233
- 3008280196
- 9611112
- 3002806953
- 3036795921
- 8010372
- 3012995405
- 8044098
- 3001595398
- 9710524
- 3004552850
- 1926681
- 9610905
- 3015173212
- 9611827
- 3012507533
- 3002808270
- 3043355002
- 3002807120
- 1935627
- 8010733
- 3003877407
- 3004168759
- 1421101
- 3003759558
- 3008719017
- 3006380247
- 3009513193
- 8010890
- 8040884
- 3023464160
- 8043467
- 1721676
- 3004519921
- 9611102
- 3005061536
- 3005194291
- 3007840839
- 3005809810
- 2248180
- 1054811
- 3001084743
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code JZF #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K973587 | EXMOOR TYMPANOCENTESIS KIT (TK/1) | Exmoor Plastics , Ltd. | 1998-01-23 |
| K862903 | MIDDLE EAR VIEWER AND FLUID COLLECTOR | Steven K. Juhn | 1986-11-24 |
| K853589 | SHAH SELF-CLEARING MASTOID SUCTION TUBE | Downs Surgical , Ltd. | 1985-12-23 |
| K841357 | MICRO FLUID APPLICATOR | Treace Medical, Inc. | 1984-08-24 |
Legacy Summary#
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FDA Review#
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