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#
- 9610612
- 3019404837
- 3010288346
- 3010442693
- 3009049852
- 1032227
- 2520265
- 3017352116
- 3004892425
- 1419982
- 3024946194
- 9613083
- 3042866301
- 9614069
- 3044744766
- 3002769835
- 1419489
- 3011600579
- 3008808049
- 3009703496
- 3002769844
- 8040278
- 3043047788
- 3008770655
- 9616119
- 9681622
- 9611503
- 9611367
- 3015512299
- 3003407244
- 3013946322
- 1421307
- 3014680812
- 3009255580
- 3014829979
- 3048101437
- 3007064566
- 3003644849
- 3003963832
- 3003882387
- 3012421607
- 2023950
- 3003969055
- 3030644259
- 3005440795
- 3036795921
- 3015176311
- 3010055973
- 3009968482
- 9614075
- 3014937043
- 8043554
- 3004425647
- 3049552730
- 9680735
- 3043239665
- 9610905
- 2024312
- 3043355002
- 3007751820
- 3003877407
- 3004168759
- 3038718579
- 3003759558
- 3009513193
- 3022862651
- 1422507
- 3003905396
- 1419247
- 8010155
- 9680026
- 3005831677
- 3008493350
- 3011625373
- 3029082594
- 2954705
- 3004193466
- 3005897698
- 3011499367
- 3005809810
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code EKB #
Legacy Summary#
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FDA Review#
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