FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
INTERAD 520
K Number: K833821
·
Decision Jan 13, 1984
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
129
Applicant Total
4
Review Days
72
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Basic Information
- Device Name
- INTERAD 520
- K Number
- K833821
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 892.1100
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- Interad Systems, Inc.
- Date Received
- November 2, 1983
- Decision Date
- January 13, 1984
- Product Code
- IYX
- 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 |
|---|---|---|---|
| IYX | Camera, Scintillation (Gamma) | FDA class 1 | Radiology |
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