The following data is part of a premarket notification filed by Wieland Dental + Technik Gmbh & Co. Kg with the FDA for Zirox.
Device ID | K051249 |
510k Number | K051249 |
Device Name: | ZIROX |
Classification | Powder, Porcelain |
Applicant | WIELAND DENTAL + TECHNIK GMBH & CO. KG SCHWENNINGER STRABE 13 Pforzheim, DE D-75179 |
Contact | Gerhard Polzer |
Correspondent | Gerhard Polzer WIELAND DENTAL + TECHNIK GMBH & CO. KG SCHWENNINGER STRABE 13 Pforzheim, DE D-75179 |
Product Code | EIH |
CFR Regulation Number | 872.6660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-05-16 |
Decision Date | 2005-07-22 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ZIROX 79017648 3256577 Dead/Cancelled |
Wieland Dental + Technik GmbH & Co. KG 2005-07-08 |
ZIROX 72316021 0887701 Dead/Cancelled |
NATIONAL LEAD COMPANY 1969-01-07 |