Stackhouse Assoc.
Country not established
- Devices
- 5
What Stackhouse Assoc. makes
Stackhouse Assoc. makes laser fume evacuation systems, smoke filtration systems, surgical helmet systems, and anti-infection shields, including the Modified Biovac:LFA Laser Fume Evacuation System, Airsafe Minivac Smoke Filtration System, Freedom Mark III Surgical Helmet System, and Biovac:LFA Laser Fume (Smoke) Evacuation.
These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Modified Biovac:lfa Laser Fume Evacuation System Ref K874512
Regimes: 510(k) Registry: 510(k)Anti-Infection Shield Ref K872935
Regimes: 510(k) Registry: 510(k)Airsafe Minivac Smoke Filtration System Ref K912651
Regimes: 510(k) Registry: 510(k)Freedom Mark Iii Surgical Helmet System Ref K910515
Regimes: 510(k) Registry: 510(k)Biovac: Lfa Laser Fume (Smoke) Evacuatio Ref K790877
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stackhouse Assoc. have in the registry?
The registry currently lists 5 devices for Stackhouse Assoc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stackhouse Assoc.'s devices?
Among its 5 most recently registered devices, Stackhouse Assoc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Stackhouse Assoc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Stackhouse Assoc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stackhouse Assoc. in the registry?
The most recently registered devices listed for Stackhouse Assoc. include MODIFIED BIOVAC:LFA LASER FUME EVACUATION SYSTEM, ANTI-INFECTION SHIELD, AIRSAFE MINIVAC SMOKE FILTRATION SYSTEM and FREEDOM MARK III SURGICAL HELMET SYSTEM.