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

EUM 100PRO

K Number: K131889 · Decision Apr 23, 2014
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
9
Applicant Total
16
Review Days
302

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Basic Information

Device Name
EUM 100PRO
K Number
K131889
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.2720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Promedic, Inc.
Date Received
June 25, 2013
Decision Date
April 23, 2014
Product Code
OSP
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
OSP Uterine Electromyographic Monitor

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Other Clearances by Promedic, Inc.

K Number Device Name
K112318 CLEARPATH 24
K072756 NON-IV ADAPTER FOR INFANT NG TUBE
K060497 BABYAIR
K060842 REVJET TURBO
K052903 PEDIATRIC FEEDING TUBE
K031409 URINARY CATHETERS
K024190 FENESTRATED INFUSION CATHETER
K023579 GAS SAMPLING LINES
K020005 INFANT FEEDING TUBES
K970102 FILTER
Search all 16 clearances from Promedic, Inc. →