FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇦 Canada
AQUEOUS ACRYLIC DISPERSION 28% W/W
K Number: K023671
·
Decision Nov 25, 2002
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
137
Applicant Total
1
Review Days
24
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Basic Information
- Device Name
- AQUEOUS ACRYLIC DISPERSION 28% W/W
- K Number
- K023671
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 872.3260
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Chx Technologies, Inc.
- Date Received
- November 1, 2002
- Decision Date
- November 25, 2002
- Product Code
- LBH
- 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 |
|---|---|---|---|
| LBH | Varnish, Cavity | FDA class 2 | Dental |
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