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

PROVIPONT C&B

K Number: K941849 · Decision Aug 17, 1994
Classifications
1
FEI Numbers
180
Registration Numbers
180
Same Product Code
188
Applicant Total
11
Review Days
125

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Basic Information

Device Name
PROVIPONT C&B
K Number
K941849
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3770
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ivoclar USA, Inc.
Date Received
April 14, 1994
Decision Date
August 17, 1994
Product Code
EBG
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
EBG Crown And Bridge, Temporary, Resin

Similar 510(k) Clearances

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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
K923644 DW243-64
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. →