Medical Device Manufacturer · US , Parsippany , NJ

Ebi, L.P. - FDA 510(k) Cleared Devices

95 submissions · 94 cleared · Since 1997
95
Total
94
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ebi, L.P. Anesthesiology ✕
2 devices
1-2 of 2
Cleared Aug 29, 2003
MODIFICATION TO EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM
K032390 · BSO
Anesthesiology · 25d
Cleared Dec 13, 2002
EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM
K023233 · BSO
Anesthesiology · 77d
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