K-Med, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
What K-Med, Inc. makes
K-Med, Inc. manufactures silicone sump drains with and without sheaths, designed for medical drainage applications, as well as an incentive spirometer to encourage deep breathing post-surgery. The company also produces coaxial electrodes for medical use.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
K-Med Silicone Sump Drain W/ Sheath Ref K812025
510(k) 510(k)K-Med Silicone Sump Drain Ref K812026
510(k) 510(k)K-Med Encourager Incentive Spirometer Ref K810641
510(k) 510(k)Coaxial Electrode #300A Ref K832566
510(k) 510(k)
Frequently asked questions
How many devices does K-Med, Inc. have in the registry?
The registry currently lists 4 devices for K-Med, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list K-Med, Inc.'s devices?
Among its 4 most recently registered devices, K-Med, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do K-Med, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for K-Med, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from K-Med, Inc. in the registry?
The most recently registered devices listed for K-Med, Inc. include K-MED SILICONE SUMP DRAIN W/ SHEATH, K-MED SILICONE SUMP DRAIN, K-MED ENCOURAGER INCENTIVE SPIROMETER and COAXIAL ELECTRODE #300A.