FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇦 Canada
CAPCADDY
K Number: K880621
·
Decision Apr 18, 1988
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
44
Applicant Total
1
Review Days
62
Basic Information
- Device Name
- CAPCADDY
- K Number
- K880621
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.6770
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- CAPCAD, INC.
- Date Received
- February 16, 1988
- Decision Date
- April 18, 1988
- Product Code
- EJI
- 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 |
|---|---|---|---|
| EJI | Syringe, Cartridge | FDA class 2 | Dental |
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