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#
- 3023657851
- 9611112
- 3007507973
- 8010372
- 3004215117
- 9615857
- 1421879
- 1056350
- 3009703496
- 3006098219
- 2511556
- 3003761012
- 1932214
- 8040278
- 3010041511
- 1923569
- 9611827
- 3008338766
- 3016825318
- 8040263
- 8010733
- 9611283
- 9613926
- 9612501
- 3015173212
- 3014437893
- 8040881
- 1054811
- 3002806953
- 3008044484
- 3004519921
- 8039051
- 3003759558
- 1313525
- 3006142527
- 3001595398
- 3012507533
- 3009255580
- 8010343
- 3002808270
- 3001620590
- 3006380247
- 2521453
- 3024988980
- 3004168759
- 3003965134
- 3007583964
- 8041151
- 3004001706
- 1836161
- 3002858762
- 3004571672
- 3010726901
- 3007840839
- 8020659
- 3011050570
- 3035708926
- 9680515
- 3015946389
- 9680837
- 3010288346
- 1526854
- 2529846
- 8044098
- 8040884
- 9611062
- 3013503739
- 1057421
- 3003418325
- 1828464
- 3003700106
- 8010890
- 3023464160
- 3011137372
- 3026848699
- 3007137643
- 1649518
- 1037007
- 3010353847
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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