FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DIAGNOSOFT HARP
K Number: K061368
·
Decision Jul 28, 2006
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
3
Review Days
73
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Basic Information
- Device Name
- DIAGNOSOFT HARP
- K Number
- K061368
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1000
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Diagnosoft, Inc.
- Date Received
- May 16, 2006
- Decision Date
- July 28, 2006
- Product Code
- LNH
- 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 |
|---|---|---|---|
| LNH | System, Nuclear Magnetic Resonance Imaging | FDA class 2 | Radiology |
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