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

DENTURE PLASTIC TEETH

K Number: K924526 · Decision Nov 4, 1992
Classifications
1
FEI Numbers
99
Registration Numbers
99
Same Product Code
54
Applicant Total
10
Review Days
57

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Basic Information

Device Name
DENTURE PLASTIC TEETH
K Number
K924526
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3590
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Austenal, Inc.
Date Received
September 8, 1992
Decision Date
November 4, 1992
Product Code
ELM
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
ELM Denture, Plastic, Teeth

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Other Clearances by Austenal, Inc.

K Number Device Name
K011674 DC - CRISTAL
K001799 DC-TELL
K001815 DC ZIRKON
K001798 DC TITAN
K970522 MYERSON'S ECONOMY DENTURE BASE MATERIAL
K970205 VITALLIUM 2000 ALLOY; VITALLIUM 2000 PLUS ALLOY; COBALT CHROME CASTING ALLOY
K955509 MIDAS GOLD ELECTROFORMING SYSTEM
K954810 MYERSON IR DENTURE BASE
K933468 MYERSON'S PERMASOFT SOFT RELINE MATERIAL