FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DW243-64

K Number: K923644 · Decision Nov 4, 1992
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
193
Applicant Total
11
Review Days
106

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Basic Information

Device Name
DW243-64
K Number
K923644
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3060
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ivoclar USA, Inc.
Date Received
July 21, 1992
Decision Date
November 4, 1992
Product Code
EJS
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EJS Alloy, Other Noble Metal

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Other Clearances by Ivoclar USA, Inc.

K Number Device Name
K012877 HIGH GOLD PALLADIUM FREE CERAMIC SOLDER
K981264 ARISTON PHC
K980986 PROCAD
K941849 PROVIPONT C&B
K864708 SR 3/60 NF DENTURE MATER. & SELF-CURE DENT. RESIN
K864710 ISOSIT N
K864707 SR-VIVODENT ANTERIOR & SR-ORTHOTYP POSTERIOR TEETH
K864709 IVOCRYL HEAT CURE & IVOCRYL QUICK DENTURE MATERIAL
K863421 SR-IVOLEN TRAY MATERIAL
K844349 SR VIVODENT PE ANTERIOR TEETH & SR ORTHOTYP RE POS
Search all 11 clearances from Ivoclar USA, Inc. →