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

DC TITAN

K Number: K001798 · Decision Jul 31, 2000
Classifications
1
FEI Numbers
94
Registration Numbers
94
Same Product Code
152
Applicant Total
10
Review Days
47

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Basic Information

Device Name
DC TITAN
K Number
K001798
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3710
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Austenal, Inc.
Date Received
June 14, 2000
Decision Date
July 31, 2000
Product Code
EJH
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
EJH Alloy, Metal, Base

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Other Clearances by Austenal, Inc.

K Number Device Name
K011674 DC - CRISTAL
K001799 DC-TELL
K001815 DC ZIRKON
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
K924526 DENTURE PLASTIC TEETH