FDA 510(k)
FDA unclassified
Substantially Equivalent
🇰🇷 South Korea
I-ROOT 100
K Number: K112508
·
Decision Jun 19, 2012
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
45
Applicant Total
4
Review Days
294
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Basic Information
- Device Name
- I-ROOT 100
- K Number
- K112508
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- S-Denti Co., Ltd.
- Date Received
- August 30, 2011
- Decision Date
- June 19, 2012
- Product Code
- LQY
- Advisory Committee
- Unknown
- 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 |
|---|---|---|---|
| LQY | Locator, Root Apex | FDA unclassified | Unknown |
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