Electrochemical Drug Delivery, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Electrochemical Drug Delivery, Inc. makes
Electrochemical Drug Delivery, Inc. manufactures the INFU.DISK, a device designed for controlled electrochemical drug delivery, and the UNI-DOSE SYRINGE PUMP, a programmable syringe pump for precise medication administration.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. These products are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Infu.disk Ref K904619
Regimes: 510(k) Registry: 510(k)Uni-Dose Syringe Pump Ref K920013
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Electrochemical Drug Delivery, Inc. have in the registry?
The registry currently lists 2 devices for Electrochemical Drug Delivery, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Electrochemical Drug Delivery, Inc.'s devices?
Among its 2 most recently registered devices, Electrochemical Drug Delivery, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Electrochemical Drug Delivery, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Electrochemical Drug Delivery, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Electrochemical Drug Delivery, Inc. in the registry?
The most recently registered devices listed for Electrochemical Drug Delivery, Inc. include INFU.DISK and UNI-DOSE SYRINGE PUMP.