FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
C-ARM TABLE IVS-100
K Number: K963888
·
Decision Dec 18, 1996
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
297
Applicant Total
90
Review Days
83
Basic Information
- Device Name
- C-ARM TABLE IVS-100
- K Number
- K963888
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1650
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- SHIMADZU MEDICAL SYSTEMS
- Date Received
- September 26, 1996
- Decision Date
- December 18, 1996
- Product Code
- JAA
- 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 |
|---|---|---|---|
| JAA | System, X-Ray, Fluoroscopic, Image-Intensified | FDA class 2 | Radiology |
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