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

RMGI LOW VISCOSITY

K Number: K123265 · Decision Dec 7, 2012
Classifications
1
FEI Numbers
144
Registration Numbers
144
Same Product Code
504
Applicant Total
32
Review Days
49

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Basic Information

Device Name
RMGI LOW VISCOSITY
K Number
K123265
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pulpdent Corporation
Date Received
October 19, 2012
Decision Date
December 7, 2012
Product Code
EMA
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
EMA Cement, Dental

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