Med Institute, Inc.
West Lafayette, IN, US
Med Institute, Inc. appears in FDA device records in West Lafayette, IN. FDA records list 26 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 26
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 26 510(k) clearances for Med Institute, Inc. between 1990 and 2000. The busiest year on record is 1991, with 6. The most recent is 2000, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1990 | 1 |
| 1991 | 6 |
| 1992 | 3 |
| 1993 | 3 |
| 1994 | 2 |
| 1995 | 3 |
| 1996 | 1 |
| 1997 | 3 |
| 1998 | 3 |
| 2000 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K990034 | WILSON-COOK COLONIC Z-STENT | MQR | Substantially Equivalent | |
| K982507 | MINI POLYURETHANE CATHETER | LJT | Substantially Equivalent | |
| K981061 | INTRAVASCULAR RETRIEVAL DEVICE | GCC | Substantially Equivalent | |
| K964001 | SWARTZ DOPPLER FLOW PROBE AND MONITOR SYSTEM | ITX | Substantially Equivalent | |
| K971140 | VITAL-PORT INFUSION PAL | LJT | Substantially Equivalent | |
| K970442 | TARGET VITAL-PORT VASCULAR ACCESS SYSTEM | LJT | Substantially Equivalent | |
| K945586 | FLEXIBLE DILATING SHEATH | DRE | Substantially Equivalent | |
| K960698 | NON-CORING NEEDLE | FMI | Substantially Equivalent | |
| K941228 | ENDOLUMINAL ACCESS TUBE | KNT | Unknown | |
| K951077 | VITAL-PORT PETIET POLYSULFONE VASCULAR ACCESS SYSTEM | LJT | Substantially Equivalent | |
| K951076 | VITAL-PORT PETITE DUAL VASCULAR ACCESS SYSTEM | LJT | Substantially Equivalent | |
| K932411 | VITAL-PORT VASC ACCESS SYS W/DUAL LUM INJECTROL CA | LJT | Substantially Equivalent | |
| K934520 | VITAL-PORT VASCULAR ACCESS SYSTEM | LJT | Substantially Equivalent | |
| K931586 | VITAL-PORT MINI VASCULAR ACCESS SYSTEM | DWF | Unknown | |
| K924748 | VITAL-PORT VASC ACCESS 901OP/911OP/9012P/9112P | LJT | Substantially Equivalent | |
| K922896 | VITAL-PORT VASCULAR ACCESS SYSTEM W/ INJECTROL | LJT | Unknown | |
| K922354 | BYRD TELESCOPING STAINLESS STEEL DILAT SHEATH SET | GCC | Substantially Equivalent | |
| K921201 | VITAL-PORT M.R.I. DUAL LUMEN VASCULAR ACCESS SYST. | LJT | Substantially Equivalent | |
| K914555 | WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL (MODI) | DRE | Substantially Equivalent | |
| K913350 | VITAL-PORT(R) PETITE VASCULAR ACCESS SYSTEM | LJT | Substantially Equivalent | |
| K912465 | VITAL-PORT DUAL LUMEN VASCULAR ACCESS SYSTEM 1121 | LJT | Substantially Equivalent | |
| K912424 | VITAL-PORT VASCULAR ACCESS SYSTEM 7010 AND 7110 | LJT | Substantially Equivalent | |
| K912423 | VITAL-PORT M.R.I. VASCULAR ACCESS SYSTEM 7012,7112 | LJT | Substantially Equivalent | |
| K911449 | VITAL-PORT VASCULAR ACCESS SYSTEM | LJT | Substantially Equivalent | |
| K910005 | VITAL-PORT(TM) M.R.I. VASCULAR ACCESS SYSTEM | LJT | Substantially Equivalent | |
| K904077 | VITAL-PORT DUAL LUMEN VASCULAR ACCESS SYSTEM | LJT | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- DWFCatheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
- GCCDilator, Catheter
- DREDilator, Vessel, For Percutaneous Catheterization
- FMINeedle, Hypodermic, Single Lumen
- LJTPort & Catheter, Implanted, Subcutaneous, Intravascular
- MQRStent, Colonic, Metallic, Expandable
- ITXTransducer, Ultrasonic, Diagnostic
- KNTTubes, Gastrointestinal (And Accessories)
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain