FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
EXAFLEX IMPRESSION MATERIAL (MODIFICATION)
K Number: K955932
·
Decision Mar 11, 1996
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
399
Applicant Total
98
Review Days
89
Basic Information
- Device Name
- EXAFLEX IMPRESSION MATERIAL (MODIFICATION)
- K Number
- K955932
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3660
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- GC AMERICA, INC.
- Date Received
- December 13, 1995
- Decision Date
- March 11, 1996
- Product Code
- ELW
- 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 |
|---|---|---|---|
| ELW | Material, Impression | FDA class 2 | Dental |
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