Modec Co., Inc.
Country not established
- Devices
- 1
What Modec Co., Inc. makes
Modec Co., Inc. manufactures the LILY I.V. SET, a peripheral intravenous (IV) administration device designed for fluid infusion in clinical settings.
The LILY I.V. SET is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Lily I.V. Set Ref K884657
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Modec Co., Inc. have in the registry?
The registry currently lists 1 device for Modec Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Modec Co., Inc.'s devices?
Among its 1 most recently registered device, Modec Co., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Modec Co., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Modec Co., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Modec Co., Inc. in the registry?
The most recently registered devices listed for Modec Co., Inc. include LILY I.V. SET.