FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

MEDELA SYMPHONY BREAST PUMP, MODEL 024

K Number: K020518 · Decision Mar 7, 2002
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
243
Applicant Total
19
Review Days
16

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Basic Information

Device Name
MEDELA SYMPHONY BREAST PUMP, MODEL 024
K Number
K020518
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.5160
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medela, Inc.
Date Received
February 19, 2002
Decision Date
March 7, 2002
Product Code
HGX
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
Y

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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K962612 BILIBED PHOTOTHERAPY LAMP
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