Begopal 300

FDA 510(k) K983081 · Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO

Substantially Equivalent

510(k) numberK983081

Submission

Device name
Begopal 300
Applicant
Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO
Bremen, DE
Received
September 2, 1998
Decision date
October 28, 1998
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
EJS – Alloy, Other Noble Metal
Device class
Class II (moderate risk)
Regulation
21 CFR 872.3060
Specialty
Dental

Other 510(k)s with product code EJS

510(k)DeviceApplicantDecision
K041433Bright Gold XHEJS · Traditional Ivoclar Vivadent, Inc.08/19/2004SE
K040436Simidur SuperiorEJS · Traditional Wieland Dental + Technik GmbH & Co. KG03/05/2004SE
K022252Sterngold 1, Model 1127781EJS · Abbreviated Sterngold09/19/2002SE
K022469Eco E4EJS · Traditional Wieland Dental + Technik GmbH & Co. KG09/18/2002SE
K021367Sterngold 66, Model #1180230EJS · Abbreviated Sterngold05/16/2002SE
K020195Simidur S1SEJS · Traditional Wieland Dental + Technik GmbH & Co. KG03/15/2002SE
K020194Simidur KF PlusEJS · Traditional Wieland Dental + Technik GmbH & Co. KG03/15/2002SE
K020192Simidur S2EJS · Traditional Wieland Dental + Technik GmbH & Co. KG03/15/2002SE
K014042D.Sign 84EJS · Traditional Ivoclar Vivadent, Inc.02/22/2002SE
K013809D.Sign 59EJS · Traditional Ivoclar Vivadent, Inc.02/07/2002SE

More from Ivoclar Vivadent, Inc.

510(k)DeviceDecision
K132102Bece Cad Zirkon Ht+EIH · Traditional 11/12/2013SE
K123929Begopal+EJH · Abbreviated 03/14/2013SE
K090434Bece PressEIH · Traditional 07/06/2009SE

Questions and answers

When was Begopal 300 cleared by the FDA?

Begopal 300 (K983081) received a 510(k) decision of Substantially Equivalent on October 28, 1998, 56 days after the submission was received.

What is the product code of K983081?

The FDA product code is EJS – Alloy, Other Noble Metal, a Class II (moderate risk) device regulated under 21 CFR 872.3060.