The following data is part of a premarket notification filed by Espe Gmbh & Co. Kg. with the FDA for Microgliss.
Device ID | K954180 |
510k Number | K954180 |
Device Name: | MICROGLISS |
Classification | Material, Impression |
Applicant | ESPE GMBH & CO. KG. AM GRIESBERG 2 Seefeld, DE D-82229 |
Contact | Barbara Wagner |
Correspondent | Barbara Wagner ESPE GMBH & CO. KG. AM GRIESBERG 2 Seefeld, 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 | 1995-09-06 |
Decision Date | 1995-11-21 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MICROGLISS 79154739 4737228 Live/Registered |
The Swatch Group Recherche et Développement SA (The Swatch Group Forschungs- und Entwicklungs AG) (The Swatch Group 2014-10-02 |
MICROGLISS 73086788 1061088 Dead/Expired |
ESPE FABRIK PHARMAZENTISCHER PRAPARATE GMBH 1976-05-11 |