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FDA 510(k), K152952, E-Cath
FDA 510(k), K152952, E-Cath
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510(K) Number: K152952
Device Name: E-Cath
Manufacturer: PAJUNK GmbH Medizintechnologie
Device Classification Name: catheter, conduction, anesthetic
Regulation Number: 868.5120
Classification Product Code: BSO
Date Received: 10/06/2015
Decision Date: 07/13/2016
Regulation Medical Specialty: Anesthesiology
Device Name: E-Cath
Manufacturer: PAJUNK GmbH Medizintechnologie
Device Classification Name: catheter, conduction, anesthetic
Regulation Number: 868.5120
Classification Product Code: BSO
Date Received: 10/06/2015
Decision Date: 07/13/2016
Regulation Medical Specialty: Anesthesiology
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- 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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