Mason-Keller Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Mason-Keller Corp. makes
Mason-Keller Corp. produces single-use wound care and intravenous access products, including sterile dressing change kits, hydrogel and wet saline dressings, and intravenous start kits for peripheral vein access.
The company’s portfolio is regulated under FDA’s Class I, Class II, and Unclassified device categories, with relevant products listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Dressing Change Kit Ref K940069
Regimes: 510(k) Registry: 510(k)Kit, I.V. Start Ref K940035
Regimes: 510(k) Registry: 510(k)M-K Wet Saline Dressing Ref K940110
Regimes: 510(k) Registry: 510(k)M-K Hydrogel Dressing Ref K940409
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mason-Keller Corp. have in the registry?
The registry currently lists 4 devices for Mason-Keller Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mason-Keller Corp.'s devices?
Among its 4 most recently registered devices, Mason-Keller Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Mason-Keller Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Mason-Keller Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mason-Keller Corp. in the registry?
The most recently registered devices listed for Mason-Keller Corp. include DRESSING CHANGE KIT, KIT, I.V. START, M-K WET SALINE DRESSING and M-K HYDROGEL DRESSING.