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

POLYSTAR 79 DENTURE BASE RESIN

K Number: K072851 · Decision Feb 20, 2008
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
329
Applicant Total
7
Review Days
139

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Basic Information

Device Name
POLYSTAR 79 DENTURE BASE RESIN
K Number
K072851
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cmp Industries, LLC
Date Received
October 4, 2007
Decision Date
February 20, 2008
Product Code
EBI
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
EBI Resin, Denture, Relining, Repairing, Rebasing

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Other Clearances by Cmp Industries, LLC

K Number Device Name
K170423 DentureID Microchip
K170375 Nobilplast Denture Resin
K072402 FLEX-STAR V
K033020 IMPAK ACRYLIC REPAIR RESIN LIQUID
K953594 VULCAN
K902972 FLEXOR (DENTURE ACRYLIC RELINE MATERIAL)