510(k) K853698
- Device
- Scotchprime Ceramic Primer
- Applicant
- 3M COMPANY
- 510(k) number
- K853698
- Product code
- EIH
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1985-11-14
- Date received
- 1985-09-04
- Regulation
- 872.6660
- Classification name
- Powder, Porcelain
- Medical specialty
- Dental
- Review panel
- Dental
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Related Records
Applicant Contact
- Contact
- DON MCKENZIE
- Address
- Chemolite Blvd. & Washington City Rd. 19 Cottae Grove MN US 55016 55016
FDA Registration Numbers
- 3022082678
- 1410097
- 3040605150
- 3005942449
- 3023272670
- 9612352
- 2916735
- 3039433962
- 3017674095
- 3031605796
- 1420052
- 3013136463
- 3008564629
- 3015978392
- 1420089
- 3017619362
- 3031841433
- 3009727738
- 3019596325
- 3030515618
- 3018249917
- 3034729565
- 3025436468
- 3009643402
- 3014945384
- 1064583
- 3014311922
- 3009482106
- 3009300369
- 9681531
- 3012187973
- 3002889488
- 3008383146
- 3015194291
- 2436986
- 3030464310
- 3012354669
- 3031595584
- 3018252381
- 3012441963
- 9613953
- 3014980456
- 3002807050
- 3003449480
- 2023129
- 3008912871
- 3018411778
- 3035983708
- 3004884150
- 3007160911
- 3013513796
- 3020611371
- 3003775534
- 1000118628
- 2424472
- 3031886796
- 3008582406
- 3015332784
- 3038718579
- 9681199
- 3024185724
- 3010002722
- 3034244245
- 3004491043
- 3011221537
- 3008792854
- 3030621102
- 3008754429
- 3042370495
- 3009409473
- 9613348
- 3038715999
- 3006235664
- 3009081830
- 3004905070
- 3022068322
- 3004362235
- 3008347275
- 3010564008
Source Documents
510(k) summary PDF not indicated by FDA
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