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

JETLITE 5000

K Number: K051780 · Decision Jul 28, 2005
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
213
Applicant Total
52
Review Days
27

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Basic Information

Device Name
JETLITE 5000
K Number
K051780
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6070
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
J. Morita USA, Inc.
Date Received
July 1, 2005
Decision Date
July 28, 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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