FDA 510(k), K992121, EMBOLIZATION COIL SYSTEM
FDA 510(k), K992121, EMBOLIZATION COIL SYSTEM
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510(K) Number: K992121
Device Name: EMBOLIZATION COIL SYSTEM
Manufacturer: LISA WEBB
Device Classification Name: Device, Vascular, For Promoting Embolization
Regulation Number: KRD
Classification Product Code: 06/23/1999
Date Received: 12/20/1999
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: EMBOLIZATION COIL SYSTEM
Manufacturer: LISA WEBB
Device Classification Name: Device, Vascular, For Promoting Embolization
Regulation Number: KRD
Classification Product Code: 06/23/1999
Date Received: 12/20/1999
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
- 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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