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

Demi Ultra

K Number: K163064 · Decision Jul 18, 2017
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
211
Applicant Total
25
Review Days
258

Basic Information

Device Name
Demi Ultra
K Number
K163064
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.6070
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
KERR CORPORATION
Date Received
November 2, 2016
Decision Date
July 18, 2017
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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