FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ACROSEAL ROOT CANAL OR APICAL SEALER
K Number: K023976
·
Decision Jan 30, 2003
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
142
Applicant Total
1
Review Days
64
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- ACROSEAL ROOT CANAL OR APICAL SEALER
- K Number
- K023976
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3820
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Septodont S.A.S.
- Date Received
- November 27, 2002
- Decision Date
- January 30, 2003
- Product Code
- KIF
- 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 |
|---|---|---|---|
| KIF | Resin, Root Canal Filling | FDA class 2 | Dental |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (KIF), ordered by most recent decision date.
Any-Paste
FDA 510(k)
FDA Class 2
·Dental
ZenSeal Pro
FDA 510(k)
FDA Class 2
·Dental
Root canal repair materials (nRoot BP)
FDA 510(k)
FDA Class 2
·Dental
Well-Root PT
FDA 510(k)
FDA Class 2
·Dental
One-Fil Putty Injectable
FDA 510(k)
FDA Class 2
·Dental
MTA vpt
FDA 510(k)
FDA Class 2
·Dental