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FDA 510(k), K072539, CURE CATHETER
FDA 510(k), K072539, CURE CATHETER
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510(K) Number: K072539
Device Name: CURE CATHETER
Manufacturer: CURE MEDICAL LLC.
Device Classification Name: Catheter, Straight
Regulation Number: 876.5130
Classification Product Code: EZD
Date Received: 09/10/2007
Decision Date: 09/13/2007
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: CURE CATHETER
Manufacturer: CURE MEDICAL LLC.
Device Classification Name: Catheter, Straight
Regulation Number: 876.5130
Classification Product Code: EZD
Date Received: 09/10/2007
Decision Date: 09/13/2007
Regulation Medical Specialty: Gastroenterology/Urology
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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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