FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
PIO ROOT CANAL INDICATOR
K Number: K822793
·
Decision Oct 22, 1982
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
7
Applicant Total
34
Review Days
36
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Basic Information
- Device Name
- PIO ROOT CANAL INDICATOR
- K Number
- K822793
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.4565
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- National Patent Development Corp.
- Date Received
- September 16, 1982
- Decision Date
- October 22, 1982
- Product Code
- EIL
- 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 |
|---|---|---|---|
| EIL | Gauge, Depth, Instrument, Dental | FDA class 1 | Dental |
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