Zulaf, Inc.
Country not established
- Devices
- 1
What Zulaf, Inc. makes
Zulaf, Inc. manufactures SOLO TIES, which are medical devices designed for securing medical tubing and lines to prevent disconnections or accidental removal during patient care.
The company’s portfolio is classified under FDA’s Class I regulatory category and is listed via the 510(k) clearance process. Zulaf, Inc. is headquartered in the United States.
Catalogue
Solo Ties Ref K930452
510(k) 510(k)
Frequently asked questions
How many devices does Zulaf, Inc. have in the registry?
The registry currently lists 1 device for Zulaf, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zulaf, Inc.'s devices?
Among its 1 most recently registered device, Zulaf, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Zulaf, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Zulaf, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Zulaf, Inc. in the registry?
The most recently registered devices listed for Zulaf, Inc. include SOLO TIES.