FDA 510(k), K023305, KEGELMASTER 2000

FDA 510(k), K023305, KEGELMASTER 2000

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510(K) Number: K023305
Device Name: KEGELMASTER 2000
Manufacturer: KEGELMASTER 2000 LTD.
Device Classification Name: perineometer
Regulation Number: 884.1425
Classification Product Code: HIR
Date Received: 10/03/2002
Decision Date: 12/26/2002
Regulation Medical Specialty: Obstetrics/Gynecology

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