Stickman Industries, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Stickman Industries, Inc. makes
Stickman Industries, Inc. manufactures the DAYTRIPPER DIALYSATE WARMER, a device designed to heat dialysate solutions for hemodialysis procedures.
The DAYTRIPPER DIALYSATE WARMER is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Daytripper Dialysate Warmer Ref K020542
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stickman Industries, Inc. have in the registry?
The registry currently lists 1 device for Stickman Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stickman Industries, Inc.'s devices?
Among its 1 most recently registered device, Stickman Industries, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Stickman Industries, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Stickman Industries, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stickman Industries, Inc. in the registry?
The most recently registered devices listed for Stickman Industries, Inc. include DAYTRIPPER DIALYSATE WARMER.