FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇦 Canada
DCM 1.0
K Number: K011246
·
Decision May 23, 2001
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
255
Applicant Total
7
Review Days
30
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Basic Information
- Device Name
- DCM 1.0
- K Number
- K011246
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 892.5050
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Mds Nordion
- Date Received
- April 23, 2001
- Decision Date
- May 23, 2001
- Product Code
- MUJ
- 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 |
|---|---|---|---|
| MUJ | System, Planning, Radiation Therapy Treatment | FDA class 2 | Radiology |
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