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

MEDELA PUMP IN STYLE ADVANCED BREAST PUMP

K Number: K031614 · Decision Jun 6, 2003
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
243
Applicant Total
19
Review Days
14

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Basic Information

Device Name
MEDELA PUMP IN STYLE ADVANCED BREAST PUMP
K Number
K031614
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
May 23, 2003
Decision Date
June 6, 2003
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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K984589 PHOTOTHERAPY LAMP
K983552 BASIC, MEDIAN, DOMINANT, AND VARIO
K962612 BILIBED PHOTOTHERAPY LAMP
K950750 MEDELAS BREAST PUMP
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K923577 BREAST SHELLS
K901344 MEDELA BATTERY OPERATED BREAST PUMP
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