The following data is part of a premarket notification filed by Vident with the FDA for Vmk 68 And Vmk 68n Dental Porcelain Kit.
Device ID | K901862 |
510k Number | K901862 |
Device Name: | VMK 68 AND VMK 68N DENTAL PORCELAIN KIT |
Classification | Powder, Porcelain |
Applicant | VIDENT 5130 COMMERCE DR. Baldwin Park, CA 91706 |
Contact | Ray E Morrow |
Correspondent | Ray E Morrow VIDENT 5130 COMMERCE DR. Baldwin Park, CA 91706 |
Product Code | EIH |
CFR Regulation Number | 872.6660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-04-24 |
Decision Date | 1990-10-10 |