FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ACUCAM CONCEPT IV, MODELS A1222B, A1223B, A1221B, A1121B, A1222C, A10402, A10403, A10401
K Number: K000112
·
Decision Apr 13, 2000
Classifications
1
FEI Numbers
111
Registration Numbers
111
Same Product Code
283
Applicant Total
279
Review Days
90
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Basic Information
- Device Name
- ACUCAM CONCEPT IV, MODELS A1222B, A1223B, A1221B, A1121B, A1222C, A10402, A10403, A10401
- K Number
- K000112
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.6640
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Dentsply Intl.
- Date Received
- January 14, 2000
- Decision Date
- April 13, 2000
- Product Code
- EIA
- 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 |
|---|---|---|---|
| EIA | Unit, Operative Dental | FDA class 1 | Dental |
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