Interventional Therapeutics Corp.
Santa Barbara, CA, US
Interventional Therapeutics Corp. appears in FDA device records in Santa Barbara, CA. FDA records list 28 510(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
- 28
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 28 510(k) clearances for Interventional Therapeutics Corp. between 1987 and 1996. The busiest year on record is 1993, with 9. The most recent is 1996, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1987 | 1 |
| 1990 | 2 |
| 1991 | 8 |
| 1992 | 4 |
| 1993 | 9 |
| 1994 | 1 |
| 1995 | 2 |
| 1996 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K960832 | OCCLUSION BALLOON CATHETER | MJN | Substantially Equivalent | |
| K950398 | CATHETER, BALLOON TYPE | DQO | Substantially Equivalent | |
| K945588 | DISPOSABLE 1CC SYRINGE WITH LUER LOCK | FMF | Substantially Equivalent | |
| K944354 | CONTOUR EMBOLI | HCG | Substantially Equivalent | |
| K930456 | INTHERM SINGLE-STICK RADIALLY EXPANDING DILATOR | KNT | Substantially Equivalent | |
| K914866 | ITC CONTOUR EMBOLI, MODIFICATION | HCG | Substantially Equivalent | |
| K931025 | INTHERM STASIS VALVE SYSTEM | FGE | Substantially Equivalent | |
| K931278 | INTHERM SINGLE-STICK RADIALLY EXPANDING DILATOR | GCJ | Substantially Equivalent | |
| K922609 | ITC CATHETERS W/ HYDROMER | DQY | Substantially Equivalent | |
| K925876 | ITC BUNJI PLATINUM EMBOLIZATION COIL | HCG | Substantially Equivalent | |
| K925523 | ITC BUNJI PLATINUM EMBOLIZATION COIL | HCG | Substantially Equivalent | |
| K922101 | ANGIOGRAPHIC CATHETER -- MODIFICATION | DQO | Substantially Equivalent | |
| K923518 | GUIDING CATHETER | DQY | Substantially Equivalent | |
| K924451 | INTHERM SINGLE-STICK RADIALLY EXPANDING DILATOR | FGE | Substantially Equivalent | |
| K921399 | OCCLUSION BALLON CATHETER MODIFICAION | DXC | Substantially Equivalent | |
| K920324 | ITC BUNJI COIL (MODIFICATION) | HCG | Unknown | |
| K915625 | INTRODUCER CATHETER | DYB | Substantially Equivalent | |
| K912532 | ITC HIESHIMA TAPER SELECT(TM) PERCUTANEOUS CATH | DQO | Substantially Equivalent | |
| K913932 | PERCUTANEOUS DILATOR WITH SHEATH | FGE | Substantially Equivalent | |
| K913052 | ITC GUIDING CATHETER | DQY | Substantially Equivalent | |
| K912477 | ITC COAXIAL ANGIOGRAPHIC CATH SET, MODIFICATION | DQO | Substantially Equivalent | |
| K912971 | INTHERM RADIALLY EXPANDING DILATER | FGE | Substantially Equivalent | |
| K910845 | ITC ROTATING HEMOSTATIC VALVE CAT. NO. MX 1012 | DTL | Substantially Equivalent | |
| K901287 | INTHERM TEMPORARY OCCLUSION CATHETER | DYG | Substantially Equivalent | |
| K900723 | ITC BUNJI COIL | HCG | Substantially Equivalent | |
| K900757 | ITC ANGIOGRAPHIC CATHETER | DQA | Substantially Equivalent | |
| K900756 | ITC INTRODUCER CATHETER | DYB | Substantially Equivalent | |
| K871047 | RADIOPAQUE SPHERICAL EMBOLI (RSE) | HCG | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- DTLAdaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
- DYGCatheter, Flow Directed
- MJNCatheter, Intravascular Occluding, Temporary
- DQOCatheter, Intravascular, Diagnostic
- DQYCatheter, Percutaneous
- DXCClamp, Vascular
- HCGDevice, Neurovascular Embolization
- DYBIntroducer, Catheter
- GCJLaparoscope, General & Plastic Surgery
- DQAOximeter
- FGEStents, Drains And Dilators For The Biliary Ducts
- FMFSyringe, Piston
- 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