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 | Device Class | Medical Specialty |
|---|---|---|---|
| KLC | Chair, Dental, With Operative Unit | FDA class 1 | Dental |
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| K051909 | DIAGNODENT | Oct 21, 2005 | Substantially Equivalent |
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| K050019 | IN EXAM INTRAORAL DENTAL X-RAY SYSTEM | Jan 31, 2005 | Substantially Equivalent |
| K032081 | KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60 | Jul 24, 2003 | Substantially Equivalent |
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| K030607 | KAVO EVEREST G-BLANK, KAVO EVEREST G-CERAM, COATING CERAMIC LF-3-PFM, GLAZE AND COLORINGS/STAINING/SHADES | May 2, 2003 | Substantially Equivalent |
| K024214 | KAVO EVEREST TITANBLANK | Mar 12, 2003 | Substantially Equivalent |