Applied Vascular Devices, Inc.
Santa Ana, CA, US
Applied Vascular Devices, Inc. appears in FDA device records in Santa Ana, CA. FDA records list 21 510(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
- 21
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 21 510(k) clearances for Applied Vascular Devices, Inc. between 1988 and 1991. The busiest year on record is 1991, with 10. The most recent is 1991, with 10.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1988 | 3 |
| 1989 | 4 |
| 1990 | 4 |
| 1991 | 10 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K911730 | SURGICAL OBTURATOR WITH SEAL | GCJ | Substantially Equivalent | |
| K911589 | DISPOSABLE SURGICAL TROCAR WITH SEAL | GCJ | Substantially Equivalent | |
| K910339 | AVD INTIMAX OCCLUSION CATHETER | DQT | Substantially Equivalent | |
| K910372 | INTIMAX THROMBECTOMY CATHETER | DXE | Substantially Equivalent | |
| K911181 | INTIMAX(TM) IRRIGATION CATHETER | GCA | Substantially Equivalent | |
| K910493 | AVD INTIMAX CHOLANGIOGRAPHY CATHETER | FGE | Substantially Equivalent | |
| K903848 | DIAGNOSTIC INTRASCULAR CATHETER | DQO | Substantially Equivalent | |
| K905738 | OPERATIVE CHOLANGIOGRAPHIC CATHETER | FGE | Substantially Equivalent | |
| K910079 | DISPOSABLE INTRODUCER SHEATH | KDC | Substantially Equivalent | |
| K902256 | IRRIGATION CATHETER 4, 6 AND 10 FRENCH | DQY | Substantially Equivalent | |
| K904379 | SURGICAL TROCAR AND CANNULA | HET | Substantially Equivalent | |
| K901627 | ARTERIAL EMBOLECTOMY CATHETER | DXE | Substantially Equivalent | |
| K901628 | APPLIED VASCULAR DEVICES 6MM TRACTION CLIP | DXC | Substantially Equivalent | |
| K901565 | ATRAUMAX SURGICAL CLAMP MODEL FOG-5048, 75MM SIDE | DXC | Substantially Equivalent | |
| K895691 | VASCULAR CLAMP | DXC | Substantially Equivalent | |
| K895214 | HEMOSTASIS VALVE | DYB | Substantially Equivalent | |
| K890766 | CATHETER INTRODUCER SHEATH | DYB | Substantially Equivalent | |
| K891296 | ATRAUMAX(TM) SURGICAL CLAMPS | DXC | Substantially Equivalent | |
| K883909 | SURGICAL SPRING CLIPS | DSS | Substantially Equivalent | |
| K883790 | SURGICAL CLAMP INSERTS | DXC | Substantially Equivalent | |
| K880987 | INJECTOR HANDLE WITH SYRINGE | DXT | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- GCABiliary Catheter For Stone Removal That May Also Allow For Irrigation And Contrast Injection
- DXECatheter, Embolectomy
- DQOCatheter, Intravascular, Diagnostic
- DQYCatheter, Percutaneous
- DXCClamp, Vascular
- DSSClip, Vascular
- DXTInjector And Syringe, Angiographic
- KDCInstrument, Surgical, Disposable
- DYBIntroducer, Catheter
- GCJLaparoscope, General & Plastic Surgery
- HETLaparoscope, Gynecologic (And Accessories)
- DQTOccluder, Catheter Tip
- 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