FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ELEVATOR - VARIOUS
K Number: K841011
·
Decision Jun 15, 1984
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
6
Applicant Total
41
Review Days
98
Basic Information
- Device Name
- ELEVATOR - VARIOUS
- K Number
- K841011
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.4565
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- PREMIER DENTAL PRODUCTS CO.
- Date Received
- March 9, 1984
- Decision Date
- June 15, 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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