Medical Device Manufacturer · US , Irvine , CA

Interpore Cross Intl. - FDA 510(k) Cleared Devices

39 submissions · 38 cleared · Since 1998
39
Total
38
Cleared
0
Denied
FDA 510(k) Regulatory Record - Interpore Cross Intl. Gastroenterology & Urology ✕
1 devices
1-1 of 1
Cleared Jun 13, 2001
ULTRACONCENTRATOR SYSTEM
K011148 · FJI
Gastroenterology & Urology · 58d
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All39 Orthopedic 34 Anesthesiology 2 General Hospital 2 Gastroenterology & Urology 1