FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
TRIDOROS 712
K Number: K791214
·
Decision Jul 30, 1979
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
162
Applicant Total
66
Review Days
28
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Basic Information
- Device Name
- TRIDOROS 712
- K Number
- K791214
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 892.1700
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- Siemens Corp.
- Date Received
- July 2, 1979
- Decision Date
- July 30, 1979
- Product Code
- IZO
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- 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 |
|---|---|---|---|
| IZO | Generator, High-Voltage, X-Ray, Diagnostic | FDA class 1 | Radiology |
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