K-Lok, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What K-Lok, Inc. makes
K-Lok, Inc. manufactures catheter securement devices designed to immobilize peripheral intravenous catheters in place, reducing dislodgement risks. These products include both the original catheter securement device and a modified version, intended for clinical use in medical settings.
The company’s catheter securement devices are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. These products are intended for use in the United States, where they are subject to compliance with U.S. regulatory standards.
Catalogue
K-Lok Catheter Securement Device Modification Ref K935252
510(k) 510(k)K-Lok Catheter Securement Device Ref K930225
510(k) 510(k)
Frequently asked questions
How many devices does K-Lok, Inc. have in the registry?
The registry currently lists 2 devices for K-Lok, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list K-Lok, Inc.'s devices?
Among its 2 most recently registered devices, K-Lok, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do K-Lok, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for K-Lok, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from K-Lok, Inc. in the registry?
The most recently registered devices listed for K-Lok, Inc. include K-LOK CATHETER SECUREMENT DEVICE MODIFICATION and K-LOK CATHETER SECUREMENT DEVICE.