FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ORTHODONTIC. PLASTIC BRACKET PRIMER
K Number: K780028
·
Decision Jan 17, 1978
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
192
Applicant Total
331
Review Days
11
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Basic Information
- Device Name
- ORTHODONTIC. PLASTIC BRACKET PRIMER
- K Number
- K780028
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3750
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- 3M Company
- Date Received
- January 6, 1978
- Decision Date
- January 17, 1978
- Product Code
- DYH
- 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 |
|---|---|---|---|
| DYH | Adhesive, Bracket And Tooth Conditioner, Resin | FDA class 2 | Dental |
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