510(k) K823321
- Device
- DENTAL INSTRUMENTS - CARVER
- Applicant
- MILTEX, INC.
- 510(k) number
- K823321
- Product code
- EKH
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1982-11-24
- Date received
- 1982-11-08
- Regulation
- 872.4565
- Classification name
- Carver, Dental Amalgam, 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#
- 3013552516
- 3014334038
- 3015512299
- 8010704
- 3010442693
- 3001297506
- 3027615
- 1419982
- 2431166
- 8010159
- 3005067367
- 3009968482
- 3015895045
- 3004992978
- 3002808270
- 1422507
- 2246990
- 3019404837
- 3002769835
- 3010455030
- 3009171220
- 2511556
- 3014937043
- 8043622
- 3038718579
- 3004598675
- 1720747
- 3035708926
- 3006606966
- 3001146947
- 8040881
- 1416605
- 3005621335
- 3003407244
- 3011625373
- 3010288346
- 3027556548
- 9681622
- 3011279497
- 9611367
- 8040263
- 3006059835
- 3005440795
- 8040278
- 3008808049
- 1032227
- 2080222
- 3008370577
- 3003418325
- 1836161
- 3017352116
- 2521453
- 3009340886
- 3012101664
- 3022862651
- 3029082594
- 2916714
- 3006410968
- 9611283
- 3016965929
- 3002769844
- 3004892425
- 3002808149
- 3008770252
- 3003969055
- 3004193466
- 3003334541
- 3003963832
- 2183301
- 3011499367
- 3008352964
- 8041151
- 3005897698
- 9611899
- 9612086
- 3014829979
- 3003877407
- 3010155661
- 2531684
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code EKH #
Legacy Summary#
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FDA Review#
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