Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Ideas For Medicine, Inc. · Predicate Candidate Screening
15 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
140 daysmedian FDA review time
387 days90th percentile
15clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K961883 | VERSA-CATH ARTERIAL CATHETER | Ideas For Medicine, Inc. | 1997-01-13 | 243 | 0 |
| K962751 | IDEAS' DUAL PORT | Ideas For Medicine, Inc. | 1996-09-30 | 77 | 0 |
| K961716 | VASO-SAFE ARTERIAL EMBOLECTOMY CATHETE | Ideas For Medicine, Inc. | 1996-09-19 | 140 | 0 |
| K960715 | PRUITT-INAHARA CAROTID SHUNT 400-40-8F/INAHARA-PRUITT CAROTI | Ideas For Medicine, Inc. | 1996-09-09 | 201 | 0 |
| K960422 | PRUITT SAFETY OCCLUSION CATHETER | Ideas For Medicine, Inc. | 1996-08-07 | 191 | 0 |
| K954713 | DURAL-LUMEN INTRA VASCULAR BALLOON CATHETER (MODIFICATION) | Ideas For Medicine, Inc. | 1996-07-24 | 288 | 0 |
| K935964 | IDEAS OCCLUDER | Ideas For Medicine, Inc. | 1995-01-04 | 387 | 0 |
| K935023 | GODAT UTERINE MANIPULATOR INJECTOR | Ideas For Medicine, Inc. | 1995-01-04 | 441 | 0 |
| K880231 | MODIFIED PRUITT IRRIGATION & OCCLUSION CATHETER | Ideas For Medicine, Inc. | 1988-05-25 | 133 | 1 |
| K872090 | THE ROBICSEK - PRUITT AORTIC BALLOON OCCLUSION KIT | Ideas For Medicine, Inc. | 1987-10-30 | 151 | 1 |
| K872485 | CHANGE OF CATHETER BODY MATERIAL (RADIO-OPAQUE NY) | Ideas For Medicine, Inc. | 1987-08-12 | 51 | 0 |
| K872154 | MODIFIED INFO INSERTS FOR PRUITT IRRI.-OCCLU. CATH | Ideas For Medicine, Inc. | 1987-08-03 | 63 | 0 |
| K864062 | PRUITT EMBOLECTOMY/IRRIGATION CATHETER (MODIFIED) | Ideas For Medicine, Inc. | 1987-01-06 | 78 | 0 |
| K850356 | PRUITT-VASCULAR SHUNTS | Ideas For Medicine, Inc. | 1985-02-27 | 28 | 0 |
| K801359 | PRUITT VASCULAR SHUNT | Ideas For Medicine, Inc. | 1980-07-28 | 49 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda