Linemaster Switch Corp.
United Statesfrom the FDA registration address FDA establishment FEI 3001592626
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What Linemaster Switch Corp. makes
LineMaster Switch Corp. manufactures infrared wireless foot switches designed for medical and clinical environments, enabling hands-free control of equipment like imaging systems and surgical tools.
The company’s wireless foot switches are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The products are based in the United States.
Catalogue
Ir Wireless Foot Switch Ref K053510
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3001592626
- Address
- 29 PLAINE HILL RD, WOODSTOCK, CT, 06281
Frequently asked questions
How many devices does LINEMASTER SWITCH CORP. have in the registry?
The registry currently lists 1 device for LINEMASTER SWITCH CORP.. Devices recorded under merged duplicate company entries are counted once.
Which registries list LINEMASTER SWITCH CORP.'s devices?
Among its 1 most recently registered device, LINEMASTER SWITCH CORP. has devices listed in FDA 510(k) (1 device).
What risk classes do LINEMASTER SWITCH CORP.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for LINEMASTER SWITCH CORP.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from LINEMASTER SWITCH CORP. in the registry?
The most recently registered devices listed for LINEMASTER SWITCH CORP. include IR WIRELESS FOOT SWITCH.