The following data is part of a premarket notification filed by Espe Dental Ag with the FDA for Dimension Garant L, Dimension Garant L Quick.
Device ID | K000588 |
510k Number | K000588 |
Device Name: | DIMENSION GARANT L, DIMENSION GARANT L QUICK |
Classification | Material, Impression |
Applicant | ESPE DENTAL AG ESPE PLATZ Seefeld, Bavaria, DE D-82229 |
Contact | Andreas Petermann |
Correspondent | Andreas 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 | 2000-02-22 |
Decision Date | 2000-03-30 |