FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
UROSKOP A AND B
K Number: K781532
·
Decision Sep 14, 1978
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
76
Applicant Total
66
Review Days
8
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Basic Information
- Device Name
- UROSKOP A AND B
- K Number
- K781532
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1980
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- Siemens Corp.
- Date Received
- September 6, 1978
- Decision Date
- September 14, 1978
- Product Code
- IXR
- 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 |
|---|---|---|---|
| IXR | Table, Radiographic, Tilting | FDA class 2 | Radiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (IXR), ordered by most recent decision date.
VISION R/F TILTING TABLE
FDA 510(k)
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LEGACY/LEGACY-D TABLE
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CAP-35B III/CINE 275
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PHILIPS EASY DIAGNOST
FDA 510(k)
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·Radiology
ELECTROPHYSIOLOGY TILT TABLE MODEL #9660
FDA 510(k)
FDA Class 2
·Radiology
FLUOROVIEW SERIES FLUOROSCOPIC TABLES
FDA 510(k)
FDA Class 2
·Radiology
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| K963983 | E. CAM PROFILE ATTENUATION CORRECTION | Mar 31, 1997 | Substantially Equivalent |
| K941546 | SOMATOM PROJECT 059 | Sep 20, 1994 | Substantially Equivalent |