FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DENTAL MOUTH PROP.
K Number: K802696
·
Decision Nov 12, 1980
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
27
Applicant Total
3
Review Days
13
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Basic Information
- Device Name
- DENTAL MOUTH PROP.
- K Number
- K802696
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.5070
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- Trident Dental, Inc.
- Date Received
- October 30, 1980
- Decision Date
- November 12, 1980
- Product Code
- JXL
- Advisory Committee
- Neurology
- Review Advisory Committee
- NE
- 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 |
|---|---|---|---|
| JXL | Block, Bite | FDA class 2 | Neurology |
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