Atlas FDA

Access Vascular, Inc

9 FDA 510(k) clearances · Recalling firm

Sort:Newest firstOldest first

◉ Watch Access Vascular, Inc

RecordFirmDate
HydroPICC 5Fr Dual Lumen, 80cm guidewire - Basic Kit, Product Model Number 80002002 recall (Z-0114-2024)Access Vascular, Inc2023-10-13
HydroPICC 5Fr Dual Lumen Maximal Barrier Kit, Product Model Number 80002004 recall (Z-0115-2024)Access Vascular, Inc2023-10-13
HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004 recall (Z-1605-2023)Access Vascular, Inc2023-05-18
HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short term access (<30days) t recall (Z-1155-2023)Access Vascular, Inc2023-02-22
HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term access (<30days) to recall (Z-1156-2023)Access Vascular, Inc2023-02-22
HydroMID 4Fr Single Lumen - Basic Kit, Model Number 80004002 recall (Z-1129-2023)Access Vascular, Inc2023-02-10
HydroPICC 4Fr Single Lumen, 80cm Guidewire - Basic Kit, Model Number 80001002 recall (Z-1130-2023)Access Vascular, Inc2023-02-10
HydroPICC 4Fr Single Lumen, 130cm Guidewire - Basic Kit, Model Number 80001001 recall (Z-1131-2023)Access Vascular, Inc2023-02-10
Scalpel and StatLock included with HydroPICC Catheter Kit - PICC-142, Peripherally Inserte recall (Z-0199-2023)Access Vascular, Inc.2022-11-08

Track Access Vascular, Inc automatically

Every clearance here is in the API, with alerts when new ones post.