FDA 510(k)
FDA class 2
Substantially Equivalent
🇫🇷 France
SUPRASSON P MAX
K Number: K942139
·
Decision Sep 29, 1995
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
194
Applicant Total
24
Review Days
514
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Basic Information
- Device Name
- SUPRASSON P MAX
- K Number
- K942139
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.4850
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Satelec
- Date Received
- May 3, 1994
- Decision Date
- September 29, 1995
- Product Code
- ELC
- 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 |
|---|---|---|---|
| ELC | Scaler, Ultrasonic | FDA class 2 | Dental |
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