Med Institute, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
26
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K990034WILSON-COOK COLONIC Z-STENTApril 17, 2000
K982507MINI POLYURETHANE CATHETERSeptember 16, 1998
K981061INTRAVASCULAR RETRIEVAL DEVICEMay 26, 1998
K964001SWARTZ DOPPLER FLOW PROBE AND MONITOR SYSTEMApril 17, 1998
K971140VITAL-PORT INFUSION PALNovember 17, 1997
K970442TARGET VITAL-PORT VASCULAR ACCESS SYSTEMApril 30, 1997
K945586FLEXIBLE DILATING SHEATHApril 4, 1997
K960698NON-CORING NEEDLEApril 15, 1996
K941228ENDOLUMINAL ACCESS TUBESeptember 27, 1995
K951077VITAL-PORT PETIET POLYSULFONE VASCULAR ACCESS SYSTEMJuly 31, 1995
K951076VITAL-PORT PETITE DUAL VASCULAR ACCESS SYSTEMJune 13, 1995
K932411VITAL-PORT VASC ACCESS SYS W/DUAL LUM INJECTROL CASeptember 19, 1994
K934520VITAL-PORT VASCULAR ACCESS SYSTEMSeptember 6, 1994
K931586VITAL-PORT MINI VASCULAR ACCESS SYSTEMSeptember 27, 1993
K924748VITAL-PORT VASC ACCESS 901OP/911OP/9012P/9112PJuly 28, 1993
K922896VITAL-PORT VASCULAR ACCESS SYSTEM W/ INJECTROLMarch 20, 1993
K922354BYRD TELESCOPING STAINLESS STEEL DILAT SHEATH SETJuly 30, 1992
K921201VITAL-PORT M.R.I. DUAL LUMEN VASCULAR ACCESS SYST.July 21, 1992
K914555WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL (MODI)January 3, 1992
K913350VITAL-PORT(R) PETITE VASCULAR ACCESS SYSTEMAugust 9, 1991