FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

ERKA. PERFECT-ANEROID

K Number: K103637 · Decision Jun 8, 2011
Classifications
1
FEI Numbers
172
Registration Numbers
172
Same Product Code
197
Applicant Total
1
Review Days
177

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Basic Information

Device Name
ERKA. PERFECT-ANEROID
K Number
K103637
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1120
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Erka Kallmeyer Medizintechnik GmbH
Date Received
December 13, 2010
Decision Date
June 8, 2011
Product Code
DXQ
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
Y

Classifications

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

Product Code Device Name
DXQ Blood Pressure Cuff

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