FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Evenflo Premium Double Electric Breast Pump (Model 4018)

K Number: K230481 · Decision Nov 3, 2023
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
202
Applicant Total
1
Review Days
254

Basic Information

Device Name
Evenflo Premium Double Electric Breast Pump (Model 4018)
K Number
K230481
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.5160
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Evenflo Feeding, Inc.
Date Received
February 22, 2023
Decision Date
November 3, 2023
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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