FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
INSTRUMENT, DENTAL
K Number: K834072
·
Decision Feb 21, 1984
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
6
Applicant Total
5
Review Days
88
Basic Information
- Device Name
- INSTRUMENT, DENTAL
- K Number
- K834072
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.4565
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- VENTURE TECHNOLOGY, INC.
- Date Received
- November 25, 1983
- Decision Date
- February 21, 1984
- Product Code
- EMS
- 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 |
|---|---|---|---|
| EMS | Curette, Periodontic | FDA class 1 | Dental |
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