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
HGX Pump, Breast, Powered

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