FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BOSWORTH TEMPORARY RESIN
K Number: K961199
·
Decision Jun 25, 1996
Classifications
1
FEI Numbers
180
Registration Numbers
180
Same Product Code
188
Applicant Total
45
Review Days
90
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Basic Information
- Device Name
- BOSWORTH TEMPORARY RESIN
- K Number
- K961199
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3770
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Harry J. Bosworth Co.
- Date Received
- March 27, 1996
- Decision Date
- June 25, 1996
- Product Code
- EBG
- 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 |
|---|---|---|---|
| EBG | Crown And Bridge, Temporary, Resin | FDA class 2 | Dental |
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| K040547 | AEGIS ORTHO DUAL-CURED ORTHODONTIC ADHESIVE | Mar 19, 2004 | Substantially Equivalent |
| K033751 | AEGIS PIT & FISSURE SEALANT WITH ACP | Feb 5, 2004 | Substantially Equivalent |
| K031439 | ALGINATE IMPRESSION MATERIAL III (FAST & REGULAR) | Oct 2, 2003 | Substantially Equivalent |
| K031811 | PIT & FISSURE SEALANT WITH FLUORIDE | Sep 4, 2003 | Substantially Equivalent |