Medical Device Manufacturer · US , Los Angeles , CA

Exelint International, Co. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2000
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Exelint International, Co. Gastroenterology & Urology ✕
1 devices
1-1 of 1
Cleared Aug 01, 2000
A.V. FISTULA NEEDLE
K001496 · FIE
Gastroenterology & Urology · 78d
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