Americal Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Americal Corp. makes
Americal Corp. manufactures the Tracheal Tube Laser Shield Kit, a protective device designed to reduce the risk of tracheal tube damage during laser surgical procedures.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Tracheal Tube Laser Shield Kit Ref K874679
Regimes: 510(k) Registry: 510(k)Tracheal Tube Laser Shield Kit Ref K883096
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Americal Corp. have in the registry?
The registry currently lists 2 devices for Americal Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Americal Corp.'s devices?
Among its 2 most recently registered devices, Americal Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Americal Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Americal Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Americal Corp. in the registry?
The most recently registered devices listed for Americal Corp. include TRACHEAL TUBE LASER SHIELD KIT.