FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MODEL 6110B DENTAPHOR
K Number: K870118
·
Decision Apr 10, 1987
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
21
Applicant Total
68
Review Days
88
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Basic Information
- Device Name
- MODEL 6110B DENTAPHOR
- K Number
- K870118
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.1720
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Life-Tech Intl., Inc.
- Date Received
- January 12, 1987
- Decision Date
- April 10, 1987
- Product Code
- EAT
- 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 |
|---|---|---|---|
| EAT | Tester, Pulp | FDA class 2 | Dental |
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