FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SNORENTI
K Number: K032410
·
Decision Feb 28, 2005
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
26
Applicant Total
1
Review Days
574
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Basic Information
- Device Name
- SNORENTI
- K Number
- K032410
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.5570
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- James P Boyd
- Date Received
- August 4, 2003
- Decision Date
- February 28, 2005
- Product Code
- LQZ
- 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 |
|---|---|---|---|
| LQZ | Device, Jaw Repositioning | FDA class 2 | Dental |
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