FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MOUTH PROPS
K Number: K940785
·
Decision Oct 5, 1994
Classifications
1
FEI Numbers
165
Registration Numbers
165
Same Product Code
3
Applicant Total
4
Review Days
225
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Basic Information
- Device Name
- MOUTH PROPS
- K Number
- K940785
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.4565
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Worldwide Dental, Inc.
- Date Received
- February 22, 1994
- Decision Date
- October 5, 1994
- Product Code
- EIF
- 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 |
|---|---|---|---|
| EIF | Accessories, Retractor, Dental | FDA class 1 | Dental |
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