FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
GTI CLASP COVER
K Number: K913200
·
Decision Feb 3, 1992
Classifications
1
FEI Numbers
205
Registration Numbers
205
Same Product Code
913
Applicant Total
2
Review Days
201
Basic Information
- Device Name
- GTI CLASP COVER
- K Number
- K913200
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3690
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- GTI, INC.
- Date Received
- July 17, 1991
- Decision Date
- February 3, 1992
- Product Code
- EBF
- 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 |
|---|---|---|---|
| EBF | Material, Tooth Shade, Resin | FDA class 2 | Dental |
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| K Number | Device Name | ||
|---|---|---|---|
| K860347 | SUNLAMP MODELS 24N, 30R, 30RE, 37RE | Feb 12, 1986 | Substantially Equivalent |