Fisons Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Fisons Corp. makes
Fisons Corp. manufactures the FISONEB II, a device designed for controlled fluid delivery in medical procedures, and the MICROFLATOR, a microinfusion system for precise fluid administration. The SYNCHRONER (proposed tradename) appears to be a device intended for synchronized medical applications, though its exact function is not specified.
The company’s portfolio includes devices classified under FDA’s Class I and Class II categories, with regulatory submissions recorded in the FDA’s 510(k) registry. These products are subject to U.S. medical device regulations, and the company is based in the United States.
Catalogue
Fisoneb(R) Ii Ref K950206
Regimes: 510(k) Registry: 510(k)Synchroner Tm (Proposed Tradename) Ref K853350
Regimes: 510(k) Registry: 510(k)Microflator Ref K771679
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fisons Corp. have in the registry?
The registry currently lists 3 devices for Fisons Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fisons Corp.'s devices?
Among its 3 most recently registered devices, Fisons Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Fisons Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Fisons Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fisons Corp. in the registry?
The most recently registered devices listed for Fisons Corp. include FISONEB(R) II, SYNCHRONER TM (PROPOSED TRADENAME) and MICROFLATOR.