FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

UNIVERSAL, AESTHETICA, NATEA, NATURA

K Number: K083670 · Decision Jul 23, 2009
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
3
Review Days
224

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Basic Information

Device Name
UNIVERSAL, AESTHETICA, NATEA, NATURA
K Number
K083670
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Euroteknika
Date Received
December 11, 2008
Decision Date
July 23, 2009
Product Code
DZE
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
DZE Implant, Endosseous, Root-Form

Similar 510(k) Clearances

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Other Clearances by Euroteknika

K Number Device Name
K232383 iPhysio® System
K083669 OBI