FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DIAGNODENT
K Number: K051909
·
Decision Oct 21, 2005
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
23
Applicant Total
20
Review Days
99
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Basic Information
- Device Name
- DIAGNODENT
- K Number
- K051909
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.1745
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Kavo America
- Date Received
- July 14, 2005
- Decision Date
- October 21, 2005
- Product Code
- NBL
- 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 |
|---|---|---|---|
| NBL | Laser, Fluorescence Caries Detection | FDA class 2 | Dental |
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Other Clearances by Kavo America
| K Number | Device Name | ||
|---|---|---|---|
| K073074 | KEY LASER III 1243 US WITH DETECT | Jul 10, 2008 | Substantially Equivalent |
| K072262 | GENTLERAY 980 DIODE LASER SYSTEM | Oct 26, 2007 | Substantially Equivalent |
| K063624 | KAVO EVEREST C-TEMP | Feb 8, 2007 | Substantially Equivalent |
| K030146 | KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+ | Aug 3, 2005 | Substantially Equivalent |
| 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 |
| K031868 | PROPHYPEARLS | Jul 9, 2003 | Substantially Equivalent |
| 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 |
| K012308 | KAVO QUATTROCARE | Jun 26, 2002 | Substantially Equivalent |