FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
PERIODONTAL PROBE - AUTOPROBE
K Number: K880209
·
Decision Apr 27, 1988
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
7
Applicant Total
279
Review Days
103
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Basic Information
- Device Name
- PERIODONTAL PROBE - AUTOPROBE
- K Number
- K880209
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.4565
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Dentsply Intl.
- Date Received
- January 15, 1988
- Decision Date
- April 27, 1988
- 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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