510(k) K014082

Device
D.SIGN 53, MODEL NA1012204
Applicant
Ivoclar Vivadent, Inc.
510(k) number
K014082
Product code
EJS
Decision
Substantially Equivalent (SESE)
Decision date
2002-01-30
Date received
2001-12-11
Regulation
872.3060
Classification name
Alloy, Other Noble Metal
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
N

Applicant Contact#

Contact
DONNA M HARTNETT
Address
175 Pineview Dr. Amherst NY US 14228 14228

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code EJS#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K041433BRIGHT GOLD XHIvoclar Vivadent, Inc.2004-08-19
K040436SIMIDUR SUPERIORWieland Dental + Technik GmbH & Co. KG2004-03-05
K022252STERNGOLD 1, MODEL 1127781Sterngold2002-09-19
K022469ECO E4Wieland Dental + Technik GmbH & Co. KG2002-09-18
K021367STERNGOLD 66, MODEL #1180230Sterngold2002-05-16
K020192SIMIDUR S2Wieland Dental + Technik GmbH & Co. KG2002-03-15
K020194SIMIDUR KF PLUSWieland Dental + Technik GmbH & Co. KG2002-03-15
K020195SIMIDUR S1SWieland Dental + Technik GmbH & Co. KG2002-03-15
K014042D.SIGN 84Ivoclar Vivadent, Inc.2002-02-22
K013809D.SIGN 59Ivoclar Vivadent, Inc.2002-02-07
K012841DUO PAL 6, ORDER-NO.: 2154Wieland Edelmetalle GmbH & Co.2001-11-20
K012828PORTA SMK 82, MODEL 2032Wieland Edelmetalle GmbH & Co.2001-11-01
K012840EURO 45, ORDER-NO.: 2064Wieland Edelmetalle GmbH & Co.2001-10-23
K012303JEL-20J.F. Jelenko & Co., Inc.2001-08-22
K003632DW 273 #1Ivoclar North America, Inc.2000-12-20