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FDA 510(k), K943801, URIGLOW TRANSILLUMINATING URETERIC STENT MODEL
FDA 510(k), K943801, URIGLOW TRANSILLUMINATING URETERIC STENT MODEL
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510(K) Number: K943801
Device Name: URIGLOW TRANSILLUMINATING URETERIC STENT MODEL
Manufacturer: ROCKET OF LONDON, LTD.
Device Classification Name: light, catheter, fiberoptic, glass, ureteral
Regulation Number: 876.4020
Classification Product Code: FCS
Date Received: 08/03/1994
Decision Date: 08/15/1995
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: URIGLOW TRANSILLUMINATING URETERIC STENT MODEL
Manufacturer: ROCKET OF LONDON, LTD.
Device Classification Name: light, catheter, fiberoptic, glass, ureteral
Regulation Number: 876.4020
Classification Product Code: FCS
Date Received: 08/03/1994
Decision Date: 08/15/1995
Regulation Medical Specialty: Gastroenterology/Urology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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