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FDA 510(k), K191503, MobileRay Pulse SE Digital Imaging System
FDA 510(k), K191503, MobileRay Pulse SE Digital Imaging System
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510(K) Number: K191503
Device Name: MobileRay Pulse SE Digital Imaging System
Manufacturer: Terry Ancar
Device Classification Name: Interventional Fluoroscopic X-Ray System
Regulation Number: OWB
Classification Product Code: KXA
Date Received: 06/06/2019
Decision Date: 09/04/2019
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology
Device Name: MobileRay Pulse SE Digital Imaging System
Manufacturer: Terry Ancar
Device Classification Name: Interventional Fluoroscopic X-Ray System
Regulation Number: OWB
Classification Product Code: KXA
Date Received: 06/06/2019
Decision Date: 09/04/2019
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology
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- 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.
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