510(k) K821780
- Device
- BEACH EXPLORER NO. 23T.G.
- Applicant
- PACIFIC DENTAL CORP.
- 510(k) number
- K821780
- Product code
- EKB
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1982-07-06
- Date received
- 1982-06-17
- Regulation
- 872.4565
- Classification name
- Explorer, Operative
- Medical specialty
- Dental
- Review panel
- Dental
- 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
- 3030644259
- 3038718579
- 3005440795
- 3004425647
- 2431166
- 2080222
- 3006059835
- 1421879
- 3009703496
- 3004892425
- 3003038445
- 2511556
- 8040278
- 2023950
- 3012101664
- 8010099
- 3009049852
- 3003963832
- 3008797953
- 3008338766
- 9611283
- 3004193466
- 3004598675
- 8040881
- 3010055973
- 3003759558
- 8010159
- 3001146947
- 3009340886
- 3015895045
- 3006536571
- 3009255580
- 3008808049
- 3001297506
- 3027556548
- 1032347
- 3003120666
- 2521453
- 3004168759
- 8010704
- 3015176311
- 9611899
- 3002769844
- 3013946322
- 3014937043
- 8041151
- 3013358456
- 1836161
- 3013022399
- 9614075
- 3029082594
- 3035708926
- 9680515
- 1419489
- 3003644849
- 3010288346
- 8010155
- 3012421607
- 3005092287
- 1419982
- 1422507
- 9611062
- 9611503
- 9680244
- 3003418325
- 1421307
- 1419247
- 9611367
- 3013547731
- 2520265
- 3013497507
- 3008493350
- 2085199
- 3004992978
- 3011625373
- 8043554
- 2024312
- 3014829979
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code EKB #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K851724 | 1410/1 TO 1435/13 VARIOUS PROBES & EXPLORERS | Artiberia | 1985-07-02 |
Legacy Summary#
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FDA Review#
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