Ideas for Medicine, Inc.
Walker, MI, US
Ideas For Medicine, Inc. appears in FDA device records in Walker, MI. FDA records list 15 510(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
- 15
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 15 510(k) clearances for Ideas for Medicine, Inc. between 1980 and 1997. The busiest year on record is 1996, with 5. The most recent is 1997, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1980 | 1 |
| 1985 | 1 |
| 1987 | 4 |
| 1988 | 1 |
| 1995 | 2 |
| 1996 | 5 |
| 1997 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K961883 | VERSA-CATH ARTERIAL CATHETER | DXE | Substantially Equivalent | |
| K962751 | IDEAS' DUAL PORT | LJT | Substantially Equivalent | |
| K961716 | VASO-SAFE ARTERIAL EMBOLECTOMY CATHETE | DXE | Substantially Equivalent | |
| K960715 | PRUITT-INAHARA CAROTID SHUNT 400-40-8F/INAHARA-PRUITT CAROTID SHUNT 500-50-8F | MJN | Substantially Equivalent | |
| K960422 | PRUITT SAFETY OCCLUSION CATHETER | MJN | Substantially Equivalent | |
| K954713 | DURAL-LUMEN INTRA VASCULAR BALLOON CATHETER (MODIFICATION) | FGE | Substantially Equivalent | |
| K935964 | IDEAS OCCLUDER | DXC | Substantially Equivalent | |
| K935023 | GODAT UTERINE MANIPULATOR INJECTOR | LKF | Substantially Equivalent | |
| K880231 | MODIFIED PRUITT IRRIGATION & OCCLUSION CATHETER | DQT | Substantially Equivalent | |
| K872090 | THE ROBICSEK - PRUITT AORTIC BALLOON OCCLUSION KIT | DQT | Substantially Equivalent | |
| K872485 | CHANGE OF CATHETER BODY MATERIAL (RADIO-OPAQUE NY) | DXE | Substantially Equivalent | |
| K872154 | MODIFIED INFO INSERTS FOR PRUITT IRRI.-OCCLU. CATH | DQT | Substantially Equivalent | |
| K864062 | PRUITT EMBOLECTOMY/IRRIGATION CATHETER (MODIFIED) | DXE | Substantially Equivalent | |
| K850356 | PRUITT-VASCULAR SHUNTS | DWF | Substantially Equivalent | |
| K801359 | PRUITT VASCULAR SHUNT | DWF | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- LKFCannula, Manipulator/Injector, Uterine
- DWFCatheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
- DXECatheter, Embolectomy
- MJNCatheter, Intravascular Occluding, Temporary
- DXCClamp, Vascular
- DQTOccluder, Catheter Tip
- LJTPort & Catheter, Implanted, Subcutaneous, Intravascular
- FGEStents, Drains And Dilators For The Biliary Ducts
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain