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

PLASTALGIN AND PLASTALGIN ORTHO

K Number: K032708 · Decision Nov 20, 2003
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
401
Applicant Total
9
Review Days
79

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Basic Information

Device Name
PLASTALGIN AND PLASTALGIN ORTHO
K Number
K032708
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3660
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Septodont
Date Received
September 2, 2003
Decision Date
November 20, 2003
Product Code
ELW
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
ELW Material, Impression

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