FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

KAVO SYSTEMATICA 1060

K Number: K940950 · Decision Dec 29, 1994
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
62
Applicant Total
20
Review Days
304

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Basic Information

Device Name
KAVO SYSTEMATICA 1060
K Number
K940950
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6250
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Kavo America
Date Received
February 28, 1994
Decision Date
December 29, 1994
Product Code
KLC
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
KLC Chair, Dental, With Operative Unit

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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
K024214 KAVO EVEREST TITANBLANK
Search all 20 clearances from Kavo America →