Creative Care Systems, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 7
What Creative Care Systems, Inc. makes
Creative Care Systems, Inc. manufactures catheter care kits, including the DAYPAK SYSTEM III and DAYPAK SYS VII, as well as dressing change kits for maintaining peripheral vascular access. Their portfolio also includes non-coring needle sets, non-kor winged infusion sets, non-kor access kits, and percutaneous central venous catheter insertion kits with optional CV components.
The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. These products are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Daypak System Iii Catheter Care Kit Ref K840681
510(k) 510(k)Daypak Sys Vii Catheter Care Kit Ref K840919
510(k) 510(k)Dressing Change Kit Ref K850887
510(k) 510(k)Non-Kor Winged Infusion Sets Ref K861406
510(k) 510(k)Non-Coring Needle Ref K841742
510(k) 510(k)Non-Kor Access Kits Ref K852831
510(k) 510(k)- 510(k) 510(k)
Frequently asked questions
How many devices does Creative Care Systems, Inc. have in the registry?
The registry currently lists 7 devices for Creative Care Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Creative Care Systems, Inc.'s devices?
Among its 7 most recently registered devices, Creative Care Systems, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Creative Care Systems, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Creative Care Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Creative Care Systems, Inc. in the registry?
The most recently registered devices listed for Creative Care Systems, Inc. include DAYPAK SYSTEM III CATHETER CARE KIT, DAYPAK SYS VII CATHETER CARE KIT, DRESSING CHANGE KIT and NON-KOR WINGED INFUSION SETS.