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FDA 510(k), K122926, SUREFLEX STEERABLE GUIDING SHEATH KIT
FDA 510(k), K122926, SUREFLEX STEERABLE GUIDING SHEATH KIT
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510(K) Number: K122926
Device Name: SUREFLEX STEERABLE GUIDING SHEATH KIT
Manufacturer: MEGHAL KHAKHAR
Device Classification Name: Introducer, Catheter
Regulation Number: DYB
Classification Product Code: 09/24/2012
Date Received: 01/24/2013
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: SUREFLEX STEERABLE GUIDING SHEATH KIT
Manufacturer: MEGHAL KHAKHAR
Device Classification Name: Introducer, Catheter
Regulation Number: DYB
Classification Product Code: 09/24/2012
Date Received: 01/24/2013
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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