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FDA 510(k), K992664, TFX MEDICAL STYLET CATHETER
FDA 510(k), K992664, TFX MEDICAL STYLET CATHETER
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510(K) Number: K992664
Device Name: TFX MEDICAL STYLET CATHETER
Manufacturer: TFX MEDICAL GROUP
Device Classification Name: stylet, catheter
Regulation Number: 870.1380
Classification Product Code: DRB
Date Received: 08/09/1999
Decision Date: 04/13/2000
Regulation Medical Specialty: Cardiovascular
Device Name: TFX MEDICAL STYLET CATHETER
Manufacturer: TFX MEDICAL GROUP
Device Classification Name: stylet, catheter
Regulation Number: 870.1380
Classification Product Code: DRB
Date Received: 08/09/1999
Decision Date: 04/13/2000
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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