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FDA 510(k), K183085, CoreDx™ Pulmonary Mini-Forceps
FDA 510(k), K183085, CoreDx™ Pulmonary Mini-Forceps
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$149.00 USD
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510(K) Number: K183085
Device Name: CoreDx™ Pulmonary Mini-Forceps
Manufacturer: Boston Scientific Corporation
Device Classification Name: bronchoscope (flexible or rigid)
Regulation Number: 874.4680
Classification Product Code: EOQ
Date Received: 11/06/2018
Decision Date: 03/08/2019
Regulation Medical Specialty: Ear Nose & Throat
Device Name: CoreDx™ Pulmonary Mini-Forceps
Manufacturer: Boston Scientific Corporation
Device Classification Name: bronchoscope (flexible or rigid)
Regulation Number: 874.4680
Classification Product Code: EOQ
Date Received: 11/06/2018
Decision Date: 03/08/2019
Regulation Medical Specialty: Ear Nose & Throat
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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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