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

MINI L.E.D., MODEL: MINI L.E.D., MODEL SMARTLITE MINI

K Number: K032465 · Decision Oct 21, 2003
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
213
Applicant Total
24
Review Days
71

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Basic Information

Device Name
MINI L.E.D., MODEL: MINI L.E.D., MODEL SMARTLITE MINI
K Number
K032465
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6070
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Satelec
Date Received
August 11, 2003
Decision Date
October 21, 2003
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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