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

SR-VIVODENT ANTERIOR & SR-ORTHOTYP POSTERIOR TEETH

K Number: K864707 · Decision Feb 10, 1987
Classifications
1
FEI Numbers
111
Registration Numbers
111
Same Product Code
54
Applicant Total
11
Review Days
70

Basic Information

Device Name
SR-VIVODENT ANTERIOR & SR-ORTHOTYP POSTERIOR TEETH
K Number
K864707
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3590
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
IVOCLAR USA, INC.
Date Received
December 2, 1986
Decision Date
February 10, 1987
Product Code
ELM
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
ELM Denture, Plastic, Teeth

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K941849 PROVIPONT C&B
K923644 DW243-64
K864708 SR 3/60 NF DENTURE MATER. & SELF-CURE DENT. RESIN
K864709 IVOCRYL HEAT CURE & IVOCRYL QUICK DENTURE MATERIAL
K864710 ISOSIT N
K863421 SR-IVOLEN TRAY MATERIAL
K844349 SR VIVODENT PE ANTERIOR TEETH & SR ORTHOTYP RE POS
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