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

KAVO EVEREST TITANBLANK

K Number: K024214 · Decision Mar 12, 2003
Classifications
1
FEI Numbers
94
Registration Numbers
94
Same Product Code
152
Applicant Total
20
Review Days
82

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Basic Information

Device Name
KAVO EVEREST TITANBLANK
K Number
K024214
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3710
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kavo America
Date Received
December 20, 2002
Decision Date
March 12, 2003
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 510(k) clearances with the same product code (EJH), ordered by most recent decision date.

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Other Clearances by Kavo America

K Number Device Name
K073074 KEY LASER III 1243 US WITH DETECT
K072262 GENTLERAY 980 DIODE LASER SYSTEM
K063624 KAVO EVEREST C-TEMP
K051909 DIAGNODENT
K030146 KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+
K050019 IN EXAM INTRAORAL DENTAL X-RAY SYSTEM
K032081 KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60
K031868 PROPHYPEARLS
K030607 KAVO EVEREST G-BLANK, KAVO EVEREST G-CERAM, COATING CERAMIC LF-3-PFM, GLAZE AND COLORINGS/STAINING/SHADES
K012308 KAVO QUATTROCARE
Search all 20 clearances from Kavo America →