1
/
of
0
FDA 510(k), K181372, Argos
FDA 510(k), K181372, Argos
Regular price
$89.00 USD
Regular price
Sale price
$89.00 USD
Unit price
/
per
510(K) Number: K181372
Device Name: Argos
Manufacturer: Retia Medical, LLC
Device Classification Name: Computer, Diagnostic, Pre-Programmed, Single-Function
Regulation Number: 870.1435
Classification Product Code: DXG
Date Received: 05/23/2018
Decision Date: 12/13/2018
Regulation Medical Specialty: Cardiovascular
Device Name: Argos
Manufacturer: Retia Medical, LLC
Device Classification Name: Computer, Diagnostic, Pre-Programmed, Single-Function
Regulation Number: 870.1435
Classification Product Code: DXG
Date Received: 05/23/2018
Decision Date: 12/13/2018
Regulation Medical Specialty: Cardiovascular
Couldn't load pickup availability
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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.
View full details