FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
.decimal p.d
K Number: K151369
·
Decision Aug 7, 2015
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
255
Applicant Total
4
Review Days
78
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Basic Information
- Device Name
- .decimal p.d
- K Number
- K151369
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.5050
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- .Decimal, LLC
- Date Received
- May 21, 2015
- Decision Date
- August 7, 2015
- 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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