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

ARGEN PMMA

K Number: K140894 · Decision Jul 31, 2014
Classifications
1
FEI Numbers
180
Registration Numbers
180
Same Product Code
188
Applicant Total
6
Review Days
114

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Basic Information

Device Name
ARGEN PMMA
K Number
K140894
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3770
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
The Argen Corporation
Date Received
April 8, 2014
Decision Date
July 31, 2014
Product Code
EBG
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
EBG Crown And Bridge, Temporary, Resin

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