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

CARDIOMEM

K Number: K122272 · Decision Mar 28, 2013
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
59
Applicant Total
8
Review Days
241

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Basic Information

Device Name
CARDIOMEM
K Number
K122272
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.2800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Getemed Medizin- Und Informationstechnik AG
Date Received
July 30, 2012
Decision Date
March 28, 2013
Product Code
MWJ
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MWJ Electrocardiograph, Ambulatory (Without Analysis)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MWJ), ordered by most recent decision date.

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Other Clearances by Getemed Medizin- Und Informationstechnik AG

K Number Device Name
K162023 CardioDay V2.5
K130516 CARDIODAY
K130785 SEER 1000
K063042 CARDIOMEM CM 3000-12BT
K070280 CARDIODAY, VERSION 2.0
K051686 CARDIOMEM CM 3000-12
K051471 CARDIODAY