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

DVI CURING LIGHT

K Number: K043530 · Decision Jan 25, 2005
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
211
Applicant Total
5
Review Days
35

Basic Information

Device Name
DVI CURING LIGHT
K Number
K043530
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6070
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DESIGNS FOR VISION, INC.
Date Received
December 21, 2004
Decision Date
January 25, 2005
Product Code
EBZ
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
EBZ Activator, Ultraviolet, For Polymerization

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K Number Device Name
K051786 MELIDE FIBEROPTIC LIGHT
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K013880 DAYLITE XENON LIGHT SOURCES
K801058 ILLUMINATED SPECULUM