FDA 510(k)
FDA class 2
Substantially Equivalent
🇰🇷 South Korea
Spectra 9Plus
K Number: K162415
·
Decision Mar 15, 2017
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
202
Applicant Total
1
Review Days
198
Basic Information
- Device Name
- Spectra 9Plus
- K Number
- K162415
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 884.5160
- Medical Specialty
- Obstetrics/Gynecology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Uzinmedicare Company
- Date Received
- August 29, 2016
- Decision Date
- March 15, 2017
- Product Code
- HGX
- Advisory Committee
- Obstetrics/Gynecology
- Review Advisory Committee
- OB
- 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 |
|---|---|---|---|
| HGX | Pump, Breast, Powered | FDA class 2 | Obstetrics/Gynecology |
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