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
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
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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