510(k) K841001
- Device
- EAR CURETTE, VARIOUS
- Applicant
- PREMIER DENTAL PRODUCTS CO.
- 510(k) number
- K841001
- Product code
- JYG
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1984-05-29
- Date received
- 1984-03-09
- Regulation
- 874.4420
- Classification name
- Curette, Ear
- 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#
- 8040233
- 3003244954
- 8010433
- 3015972835
- 9680718
- 3015895045
- 8010099
- 3008902714
- 1836161
- 3003877407
- 1055890
- 9611503
- 1056339
- 8041151
- 1935627
- 3006142527
- 2246990
- 2511556
- 3039414397
- 1923569
- 3029082594
- 9610773
- 3005440795
- 9611283
- 3004530184
- 3032747418
- 3016458459
- 3021680161
- 3014421917
- 3002858762
- 3023464160
- 3005067367
- 3004215117
- 3012267976
- 1526854
- 9613926
- 3003836856
- 2529846
- 1421879
- 3023657851
- 3030447506
- 8043496
- 3004001706
- 3006098219
- 1032347
- 9615857
- 3007478714
- 9680304
- 9613083
- 3010155661
- 3007507973
- 3010726901
- 1720747
- 3010455030
- 3006554912
- 3005695838
- 3011310592
- 3005739529
- 8043368
- 3011371465
- 3012507533
- 9613079
- 3003431869
- 3014334038
- 3005809810
- 3001620590
- 9612075
- 3003407244
- 3002090132
- 3009513193
- 3010829427
- 3010041511
- 3035678069
- 3011137372
- 3045853999
- 3007694978
- 9612074
- 2521453
- 3006380247
- 3014615697
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code JYG #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K932609 | EAR CURETTE | Ear Tech, Inc. | 1993-07-21 |
| K852039 | FLEX-LOOP FLEXIBLE EAR CORETTE | Bionix Corp. | 1985-06-11 |
| K841354 | CURETTE | Treace Medical, Inc. | 1984-07-06 |
| K823916 | WAX CURETTE TIP | Treace Medical, Inc. | 1983-01-21 |
| K822273 | ENT CURRETTES | Kelleher Corp. | 1982-08-30 |
| K822006 | OPERATIVE EAR CURRETTES & RELATED ITEM | Kelleher Corp. | 1982-08-12 |
Legacy Summary#
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FDA Review#
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