The following data is part of a premarket notification filed by Wieland Dental + Technik Gmbh & Co. Kg with the FDA for Simidur S1s.
Device ID | K020195 |
510k Number | K020195 |
Device Name: | SIMIDUR S1S |
Classification | Alloy, Other Noble Metal |
Applicant | WIELAND DENTAL + TECHNIK GMBH & CO. KG SCHWENNINGER STRASSE 13 Pforzheim, DE D75179 |
Contact | Gerhard Polzer |
Correspondent | Gerhard Polzer WIELAND DENTAL + TECHNIK GMBH & CO. KG SCHWENNINGER STRASSE 13 Pforzheim, DE D75179 |
Product Code | EJS |
CFR Regulation Number | 872.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-01-22 |
Decision Date | 2002-03-15 |
Summary: | summary |