FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MODIFICATION TO LINER II: SOFT RELINE LIQUID
K Number: K991687
·
Decision Oct 7, 1999
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
329
Applicant Total
4
Review Days
143
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Basic Information
- Device Name
- MODIFICATION TO LINER II: SOFT RELINE LIQUID
- K Number
- K991687
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3760
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Bosworth Co.
- Date Received
- May 17, 1999
- Decision Date
- October 7, 1999
- Product Code
- EBI
- 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 |
|---|---|---|---|
| EBI | Resin, Denture, Relining, Repairing, Rebasing | FDA class 2 | Dental |
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