Access Devices, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Access Devices, Inc. makes
Access Devices, Inc. manufactures percutaneous introducer sets for vascular access, intravenous catheter placement units, and central vein catheterization kits designed for medical procedures requiring secure venous access.
These products are regulated as Class II devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Access Percutaneous Introducer Set Ref K822834
Regimes: 510(k) Registry: 510(k)Intravenous Catheter Placement Unit & Ref K823017
Regimes: 510(k) Registry: 510(k)Central Vein Catherization Kit Ref K823758
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Access Devices, Inc. have in the registry?
The registry currently lists 3 devices for Access Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Access Devices, Inc.'s devices?
Among its 3 most recently registered devices, Access Devices, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Access Devices, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Access Devices, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Access Devices, Inc. in the registry?
The most recently registered devices listed for Access Devices, Inc. include ACCESS PERCUTANEOUS INTRODUCER SET, INTRAVENOUS CATHETER PLACEMENT UNIT & and CENTRAL VEIN CATHERIZATION KIT.