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

THERMABOND V

K Number: K926378 · Decision Nov 1, 1994
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
626
Applicant Total
2
Review Days
679

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Basic Information

Device Name
THERMABOND V
K Number
K926378
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3060
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Dentecon, Inc.
Date Received
December 22, 1992
Decision Date
November 1, 1994
Product Code
EJT
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
EJT Alloy, Gold-Based Noble Metal

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Other Clearances by Dentecon, Inc.

K Number Device Name
K911821 THERMABOND SUPERCAST NP OR THERMABOND SUPERCAST