FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
R-100-ET MANUAL COLLIMATOR
K Number: K900007
·
Decision Feb 6, 1990
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
16
Applicant Total
3
Review Days
35
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Basic Information
- Device Name
- R-100-ET MANUAL COLLIMATOR
- K Number
- K900007
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1610
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- Advantech
- Date Received
- January 2, 1990
- Decision Date
- February 6, 1990
- Product Code
- IZX
- 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 |
|---|---|---|---|
| IZX | Collimator, Manual, Radiographic | FDA class 2 | Radiology |
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