FDA 510(k), K181988, eMurmur ID

FDA 510(k), K181988, eMurmur ID

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510(K) Number: K181988
Device Name: eMurmur ID
Manufacturer: Andreas Reinisch
Device Classification Name: Stethoscope, Electronic
Regulation Number: DQD
Classification Product Code: 07/25/2018
Date Received: 04/17/2019
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular

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