FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RINN UNIVERSAL COLLIMATOR
K Number: K932134
·
Decision Jul 26, 1993
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
16
Applicant Total
5
Review Days
84
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Basic Information
- Device Name
- RINN UNIVERSAL COLLIMATOR
- K Number
- K932134
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1610
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Rinn Corp.
- Date Received
- May 3, 1993
- Decision Date
- July 26, 1993
- 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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