Armstrong Ind., Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Armstrong Ind., Inc. makes
Armstrong Ind., Inc. manufactures electrocardiograph (EKG) devices, including portable and handheld scopes like the Schiller EKG Combi MSG-IM and Miniscope MS-2, which record and display heart activity. The company also produces laryngoscopes for airway visualization and rescue breathing devices, such as the Rescuer, used in emergency medical scenarios.
These devices are regulated under FDA’s 510(k) clearance process, with most falling into Class I or Class II categories. The company’s products are listed in the FDA’s 510(k) registry, reflecting their authorised status for commercial distribution in the United States.
Catalogue
Schiller Ekg Combi Msg-Im Scope & Recorder Ref K852281
Regimes: 510(k) Registry: 510(k)Laryngoscope Ref K851705
Regimes: 510(k) Registry: 510(k)Electrocardiograph Ref K852181
Regimes: 510(k) Registry: 510(k)Rescuer Ref K822727
Regimes: 510(k) Registry: 510(k)Schiller Miniscope Ms-2 Ekg Scope Ref K852282
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Armstrong Ind., Inc. have in the registry?
The registry currently lists 5 devices for Armstrong Ind., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Armstrong Ind., Inc.'s devices?
Among its 5 most recently registered devices, Armstrong Ind., Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Armstrong Ind., Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Armstrong Ind., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Armstrong Ind., Inc. in the registry?
The most recently registered devices listed for Armstrong Ind., Inc. include SCHILLER EKG COMBI MSG-IM SCOPE & RECORDER, LARYNGOSCOPE, ELECTROCARDIOGRAPH and RESCUER.