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

SR 3/60 NF DENTURE MATER. & SELF-CURE DENT. RESIN

K Number: K864708 · Decision Feb 25, 1987
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
329
Applicant Total
11
Review Days
85

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Basic Information

Device Name
SR 3/60 NF DENTURE MATER. & SELF-CURE DENT. RESIN
K Number
K864708
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3760
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Ivoclar USA, Inc.
Date Received
December 2, 1986
Decision Date
February 25, 1987
Product Code
EBI
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
EBI Resin, Denture, Relining, Repairing, Rebasing

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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
K923644 DW243-64
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. →