FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
AD POST
K Number: K884277
·
Decision Dec 22, 1988
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
34
Applicant Total
52
Review Days
71
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Basic Information
- Device Name
- AD POST
- K Number
- K884277
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.3810
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- J. Morita USA, Inc.
- Date Received
- October 12, 1988
- Decision Date
- December 22, 1988
- Product Code
- ELR
- 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 |
|---|---|---|---|
| ELR | Post, Root Canal | FDA class 1 | Dental |
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