The following data is part of a premarket notification filed by Espe Dental Ag with the FDA for Impregum Garant L Duosoft.
Device ID | K994190 |
510k Number | K994190 |
Device Name: | IMPREGUM GARANT L DUOSOFT |
Classification | Material, Impression |
Applicant | ESPE DENTAL AG ESPE PLATZ Seefeld, Bavaria, DE D-82229 |
Contact | Andreras Petermann |
Correspondent | Andreras Petermann ESPE DENTAL AG ESPE PLATZ Seefeld, Bavaria, DE D-82229 |
Product Code | ELW |
CFR Regulation Number | 872.3660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-12-13 |
Decision Date | 2000-01-27 |
Summary: | summary |