FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DIGITAL ADD ON MULTI SYSTEM
K Number: K973710
·
Decision Dec 18, 1997
Classifications
1
FEI Numbers
84
Registration Numbers
84
Same Product Code
347
Applicant Total
3
Review Days
80
Basic Information
- Device Name
- DIGITAL ADD ON MULTI SYSTEM
- K Number
- K973710
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1680
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- SWISSRAY INTERNATIONAL, INC.
- Date Received
- September 29, 1997
- Decision Date
- December 18, 1997
- Product Code
- KPR
- 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 |
|---|---|---|---|
| KPR | System, X-Ray, Stationary | FDA class 2 | Radiology |
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