FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CROWN & BRIDGE RESIN FOR FABRICAT/DE
K Number: K820456
·
Decision Mar 19, 1982
Classifications
1
FEI Numbers
180
Registration Numbers
180
Same Product Code
188
Applicant Total
4
Review Days
28
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Basic Information
- Device Name
- CROWN & BRIDGE RESIN FOR FABRICAT/DE
- K Number
- K820456
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3770
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Rohm and Haas Co.
- Date Received
- February 19, 1982
- Decision Date
- March 19, 1982
- Product Code
- EBG
- 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 |
|---|---|---|---|
| EBG | Crown And Bridge, Temporary, Resin | FDA class 2 | Dental |
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