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#
- 9614069
- 3043355002
- 3022862651
- 3013497507
- 3003905396
- 3016965929
- 9610612
- 9611283
- 3003418325
- 3007064566
- 3006059835
- 3013552516
- 3008770252
- 8010445
- 9610905
- 2246990
- 3001297506
- 9611062
- 3005440795
- 3030671632
- 3002769835
- 3045857207
- 1413787
- 3004193466
- 3039435289
- 1032347
- 3003032798
- 8040278
- 9680515
- 8010732
- 2511556
- 1057946
- 2085199
- 3003038445
- 9611367
- 3044819802
- 8040881
- 3005621335
- 3005897698
- 3009703496
- 3009255580
- 8010155
- 3036795921
- 1032227
- 3004598675
- 1419982
- 3009513193
- 3012267976
- 3002834291
- 3009049852
- 1419247
- 8043554
- 2521453
- 3014829979
- 3013946322
- 3010442693
- 9680026
- 3007751820
- 3008338766
- 3038718579
- 1836161
- 3003882387
- 3021666757
- 3015512299
- 3004168759
- 3004425647
- 3013547731
- 1419489
- 3029082594
- 3011371465
- 1416605
- 3035708926
- 3017352116
- 3008902714
- 2916714
- 2954705
- 3010055973
- 8041151
- 3013358456
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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