Argon Medical Corp.
United StatesFDA applicant, unverified
- Devices
- 28
What Argon Medical Corp. makes
Argon Medical Corp. manufactures vascular access and interventional devices, including central venous catheters (such as the DIGICATH and CENTRAL CATHETER KIT), hemodialysis catheters (e.g., the ARGON DUAL LUMEN HEMODIALYSIS CATHETER), and specialized catheterization tools like the TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER and INTRODUCER FOR PTCA GUIDING CATHETERS. Their portfolio also includes sheaths, dilators, arterial line kits, and catheterization trays designed for procedural use in medical settings.
The company’s devices are classified under FDA’s Class I and Class II categories, with most requiring 510(k) clearance. Products are listed in the FDA’s 510(k) registry, and the manufacturer operates from the United States.
Catalogue
Search and filter all 28 devicesFrequently asked questions
How many devices does Argon Medical Corp. have in the registry?
The registry currently lists 28 devices for Argon Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Argon Medical Corp.'s devices?
Among its 28 most recently registered devices, Argon Medical Corp. has devices listed in FDA 510(k) (28 devices).
What risk classes do Argon Medical Corp.'s devices fall under?
Among its 28 most recently registered devices, the classes recorded for Argon Medical Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Argon Medical Corp. in the registry?
The most recently registered devices listed for Argon Medical Corp. include V-STICK VASCULAR ACCESS SET, DIGICATH, CENTRAL CATHETER KIT and ARGON DUAL LUMEN HEMODIALYSIS, CATHETER.