FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DVI CURING LIGHT
K Number: K043530
·
Decision Jan 25, 2005
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
211
Applicant Total
5
Review Days
35
Basic Information
- Device Name
- DVI CURING LIGHT
- K Number
- K043530
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.6070
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- DESIGNS FOR VISION, INC.
- Date Received
- December 21, 2004
- Decision Date
- January 25, 2005
- Product Code
- EBZ
- 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 |
|---|---|---|---|
| EBZ | Activator, Ultraviolet, For Polymerization | FDA class 2 | Dental |
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Other Clearances by DESIGNS FOR VISION, INC.
| K Number | Device Name | ||
|---|---|---|---|
| K051786 | MELIDE FIBEROPTIC LIGHT | Aug 15, 2005 | Substantially Equivalent |
| K032283 | DESIGNS FOR VISION FIBEROPTIC LIGHT | Aug 20, 2003 | Substantially Equivalent |
| K013880 | DAYLITE XENON LIGHT SOURCES | Dec 7, 2001 | Substantially Equivalent |
| K801058 | ILLUMINATED SPECULUM | May 28, 1980 | Substantially Equivalent |