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

EVERSTICK PERIO

K Number: K030072 · Decision Apr 10, 2003
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
329
Applicant Total
9
Review Days
92

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Basic Information

Device Name
EVERSTICK PERIO
K Number
K030072
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stick Tech , Ltd.
Date Received
January 8, 2003
Decision Date
April 10, 2003
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

Similar 510(k) Clearances

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Other Clearances by Stick Tech , Ltd.

K Number Device Name
K051953 EVERSTICK A&O
K031341 STICK FLOW
K030820 EVERSTICK POST
K021126 EVERSTICK ORTHO
K011788 EVERSTICK
K011799 EVERSTICKNET
K003334 STICK NET
K003333 STICK