Stackhouse, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Stackhouse, Inc. makes
Stackhouse, Inc. manufactures medical devices including the STACKHOUSE LENS HOOD (models SA-700/FS and SA-700/F) and the STACKHOUSE SMOKE EVACUATOR (models ST-3000 and ST 3100), as well as the FREEDOM ASPIRATOR (model 6000).
The company's devices are all classified as Class II and are listed in the FDA 510(k) registry. Stackhouse, Inc. is based in the US.
Catalogue
Stackhouse Lens Hood, Model SA-700/Fs Ref K003194
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Stackhouse Lens Hood, Model SA-700/F Ref K000605
Regimes: 510(k) Registry: 510(k)Freedom Aspirator, Model 6000 Ref K944116
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stackhouse, Inc. have in the registry?
The registry currently lists 4 devices for Stackhouse, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stackhouse, Inc.'s devices?
Among its 4 most recently registered devices, Stackhouse, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Stackhouse, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Stackhouse, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stackhouse, Inc. in the registry?
The most recently registered devices listed for Stackhouse, Inc. include STACKHOUSE LENS HOOD, MODEL SA-700/FS, STACKHOUSE SMOKE EVACUATOR, MODELS ST-3000, ST 3100, STACKHOUSE LENS HOOD, MODEL SA-700/F and FREEDOM ASPIRATOR, MODEL 6000.