FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SIEMENS SIRESKOP 4
K Number: K820111
·
Decision Feb 18, 1982
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
30
Applicant Total
66
Review Days
34
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Basic Information
- Device Name
- SIEMENS SIRESKOP 4
- K Number
- K820111
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1980
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- Siemens Corp.
- Date Received
- January 15, 1982
- Decision Date
- February 18, 1982
- Product Code
- KXJ
- 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 |
|---|---|---|---|
| KXJ | Table, Radiologic | FDA class 2 | Radiology |
Similar 510(k) Clearances
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