Innerdyne, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
FDA 510(k) Regulatory Record - Innerdyne, Inc. Cardiovascular ✕
3 devices
Cleared
May 26, 2000
INNERDYNE RADIALLY EXPANDING VASCULAR ACCESS SYSTEM (REVAS)
Cardiovascular
291d
Cleared
Sep 11, 1998
INNERDYNE RADIALLY EXPANDING VASCULAR ACCESS SYSTEM (HEPARIN COATED)
Cardiovascular
206d
Cleared
Oct 10, 1997
INNERDYNE RADIALLY EXPANDING VASCULAR ACCESS SYSTEM
Cardiovascular
85d