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FDA 510(k), K171620, PiCCO Catheter
FDA 510(k), K171620, PiCCO Catheter
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$149.00 USD
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510(K) Number: K171620
Device Name: PiCCO Catheter
Manufacturer: Ingrid Rohm
Device Classification Name: Probe, Thermodilution
Regulation Number: KRB
Classification Product Code: 06/02/2017
Date Received: 02/21/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: PiCCO Catheter
Manufacturer: Ingrid Rohm
Device Classification Name: Probe, Thermodilution
Regulation Number: KRB
Classification Product Code: 06/02/2017
Date Received: 02/21/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
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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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