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FDA 510(k), K031894, SCANTEC PAD
FDA 510(k), K031894, SCANTEC PAD
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510(K) Number: K031894
Device Name: SCANTEC PAD
Manufacturer: MARGARET J LARSON
Device Classification Name: Media, Coupling, Ultrasound
Regulation Number: MUI
Classification Product Code: 06/19/2003
Date Received: 07/18/2003
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology
Device Name: SCANTEC PAD
Manufacturer: MARGARET J LARSON
Device Classification Name: Media, Coupling, Ultrasound
Regulation Number: MUI
Classification Product Code: 06/19/2003
Date Received: 07/18/2003
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology
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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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