FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
IMPROVED TRY-IN GEL
K Number: K001899
·
Decision Aug 28, 2000
Classifications
1
FEI Numbers
205
Registration Numbers
205
Same Product Code
913
Applicant Total
106
Review Days
67
Basic Information
- Device Name
- IMPROVED TRY-IN GEL
- K Number
- K001899
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3690
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- SYBRON DENTAL SPECIALTIES, INC.
- Date Received
- June 22, 2000
- Decision Date
- August 28, 2000
- 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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