FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SPIN-SWI
K Number: K173224
·
Decision Feb 23, 2018
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
10
Review Days
143
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Basic Information
- Device Name
- SPIN-SWI
- K Number
- K173224
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1000
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Spintech, Inc.
- Date Received
- October 3, 2017
- Decision Date
- February 23, 2018
- 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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