The following data is part of a premarket notification filed by Davis Schottlander & Davis, Ltd. with the FDA for Matchmaker/propaque Porcelain.
Device ID | K960770 |
510k Number | K960770 |
Device Name: | MATCHMAKER/PROPAQUE PORCELAIN |
Classification | Teeth, Porcelain |
Applicant | DAVIS SCHOTTLANDER & DAVIS, LTD. DUNHAMS LANE Letchworth, Herts., GB Sg6 1ns |
Contact | B.d. Schottlander |
Correspondent | B.d. Schottlander DAVIS SCHOTTLANDER & DAVIS, LTD. DUNHAMS LANE Letchworth, Herts., GB Sg6 1ns |
Product Code | ELL |
CFR Regulation Number | 872.3920 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-02-26 |
Decision Date | 1996-11-19 |
Summary: | summary |