FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
GLUMA DESENSITIZER POWER GEL
K Number: K093575
·
Decision Mar 5, 2010
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
137
Applicant Total
11
Review Days
107
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Basic Information
- Device Name
- GLUMA DESENSITIZER POWER GEL
- K Number
- K093575
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3260
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Heraeus Kulzer, LLC
- Date Received
- November 18, 2009
- Decision Date
- March 5, 2010
- 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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