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

ECLIPSE WAX REMOVER

K Number: K061580 · Decision Jul 28, 2006
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
329
Applicant Total
23
Review Days
51

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Basic Information

Device Name
ECLIPSE WAX REMOVER
K Number
K061580
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentsply International
Date Received
June 7, 2006
Decision Date
July 28, 2006
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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