FDA 510(k), K181902, Codman Certas Plus Electronic Tool Kit
FDA 510(k), K181902, Codman Certas Plus Electronic Tool Kit
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510(K) Number: K181902
Device Name: Codman Certas Plus Electronic Tool Kit
Manufacturer: Nancy MacDonald
Device Classification Name: Shunt, Central Nervous System And Components
Regulation Number: JXG
Classification Product Code: 07/16/2018
Date Received: 10/25/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
Device Name: Codman Certas Plus Electronic Tool Kit
Manufacturer: Nancy MacDonald
Device Classification Name: Shunt, Central Nervous System And Components
Regulation Number: JXG
Classification Product Code: 07/16/2018
Date Received: 10/25/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
- 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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