Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Interventional Therapeutics Corp. — Predicate Candidate Screening
28 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
176 daysmedian FDA review time
337 days90th percentile
28clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K960832 | OCCLUSION BALLOON CATHETER | Interventional Therapeutics Corp. | 1996-05-29 | 90 | 0 |
| K950398 | CATHETER, BALLOON TYPE | Interventional Therapeutics Corp. | 1995-10-05 | 246 | 0 |
| K945588 | DISPOSABLE 1CC SYRINGE WITH LUER LOCK | Interventional Therapeutics Corp. | 1995-02-10 | 88 | 0 |
| K944354 | CONTOUR EMBOLI | Interventional Therapeutics Corp. | 1994-12-13 | 105 | 0 |
| K930456 | INTHERM SINGLE-STICK RADIALLY EXPANDING DILATOR | Interventional Therapeutics Corp. | 1993-11-17 | 294 | 0 |
| K914866 | ITC CONTOUR EMBOLI, MODIFICATION | Interventional Therapeutics Corp. | 1993-11-09 | 742 | 0 |
| K931025 | INTHERM STASIS VALVE SYSTEM | Interventional Therapeutics Corp. | 1993-09-28 | 211 | 0 |
| K931278 | INTHERM SINGLE-STICK RADIALLY EXPANDING DILATOR | Interventional Therapeutics Corp. | 1993-07-23 | 137 | 0 |
| K922609 | ITC CATHETERS W/ HYDROMER | Interventional Therapeutics Corp. | 1993-04-30 | 332 | 0 |
| K925876 | ITC BUNJI PLATINUM EMBOLIZATION COIL | Interventional Therapeutics Corp. | 1993-04-15 | 147 | 0 |
| K925523 | ITC BUNJI PLATINUM EMBOLIZATION COIL | Interventional Therapeutics Corp. | 1993-03-23 | 141 | 0 |
| K922101 | ANGIOGRAPHIC CATHETER -- MODIFICATION | Interventional Therapeutics Corp. | 1993-02-12 | 282 | 0 |
| K923518 | GUIDING CATHETER | Interventional Therapeutics Corp. | 1993-01-12 | 182 | 0 |
| K924451 | INTHERM SINGLE-STICK RADIALLY EXPANDING DILATOR | Interventional Therapeutics Corp. | 1992-10-23 | 52 | 0 |
| K921399 | OCCLUSION BALLON CATHETER MODIFICAION | Interventional Therapeutics Corp. | 1992-09-25 | 185 | 0 |
| K920324 | ITC BUNJI COIL (MODIFICATION) | Interventional Therapeutics Corp. | 1992-07-29 | 187 | 0 |
| K915625 | INTRODUCER CATHETER | Interventional Therapeutics Corp. | 1992-06-03 | 176 | 0 |
| K912532 | ITC HIESHIMA TAPER SELECT(TM) PERCUTANEOUS CATH | Interventional Therapeutics Corp. | 1991-12-11 | 187 | 0 |
| K913052 | ITC GUIDING CATHETER | Interventional Therapeutics Corp. | 1991-11-22 | 136 | 0 |
| K913932 | PERCUTANEOUS DILATOR WITH SHEATH | Interventional Therapeutics Corp. | 1991-11-22 | 80 | 0 |
| K912477 | ITC COAXIAL ANGIOGRAPHIC CATH SET, MODIFICATION | Interventional Therapeutics Corp. | 1991-11-05 | 154 | 0 |
| K912971 | INTHERM RADIALLY EXPANDING DILATER | Interventional Therapeutics Corp. | 1991-09-13 | 67 | 0 |
| K910845 | ITC ROTATING HEMOSTATIC VALVE CAT. NO. MX 1012 | Interventional Therapeutics Corp. | 1991-05-21 | 83 | 0 |
| K901287 | INTHERM TEMPORARY OCCLUSION CATHETER | Interventional Therapeutics Corp. | 1991-02-20 | 337 | 0 |
| K900723 | ITC BUNJI COIL | Interventional Therapeutics Corp. | 1991-02-19 | 369 | 0 |
| K900757 | ITC ANGIOGRAPHIC CATHETER | Interventional Therapeutics Corp. | 1990-08-14 | 179 | 0 |
| K900756 | ITC INTRODUCER CATHETER | Interventional Therapeutics Corp. | 1990-08-08 | 173 | 0 |
| K871047 | RADIOPAQUE SPHERICAL EMBOLI (RSE) | Interventional Therapeutics Corp. | 1987-05-22 | 66 | 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