FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
dS FootAnkle I6CH 1.5T Coil
K Number: K162177
·
Decision Sep 14, 2016
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
487
Applicant Total
29
Review Days
41
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Basic Information
- Device Name
- dS FootAnkle I6CH 1.5T Coil
- K Number
- K162177
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1000
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Invivo Corporation
- Date Received
- August 4, 2016
- Decision Date
- September 14, 2016
- Product Code
- MOS
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- Third Party
- Y
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| MOS | Coil, Magnetic Resonance, Specialty | FDA class 2 | Radiology |
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