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 |