Hakki Medical Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Hakki Medical Technologies, Inc. makes
Hakki Medical Technologies, Inc. manufactures urinary catheters, including standard-sized latex-free catheters in French sizes 14 to 26 and the Lotus No Balloon Catheter, designed for intermittent or indwelling urinary drainage.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
LotusCatheter (Lotus No Balloon Catheter) Ref K191512
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hakki Medical Technologies, Inc. have in the registry?
The registry currently lists 2 devices for Hakki Medical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hakki Medical Technologies, Inc.'s devices?
Among its 2 most recently registered devices, Hakki Medical Technologies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Hakki Medical Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hakki Medical Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hakki Medical Technologies, Inc. in the registry?
The most recently registered devices listed for Hakki Medical Technologies, Inc. include HAKKI URINARY CATHETER; SIZE 14, 16, 18, 20, 22, 24, 26 FRENCH and LotusCatheter (Lotus No Balloon Catheter).