Midwest Analog & Digital, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Midwest Analog & Digital, Inc. makes
Midwest Analog & Digital, Inc. manufactures medical devices for cardiac monitoring and arrhythmia analysis, including programmable modules for arrhythmia detection, strip chart recorders with integrated printers, and bedside patient monitors with modular functionality.
The company’s products are regulated under FDA 510(k) clearance, with devices classified as Class I and Class II. These devices are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Arrhythmia Program Module Ref K780432
Regimes: 510(k) Registry: 510(k)Recorder, Strip Chart With Printer Ref K781873
Regimes: 510(k) Registry: 510(k)Bedside Patient Monitor W/Modules Ref K850619
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Midwest Analog & Digital, Inc. have in the registry?
The registry currently lists 3 devices for Midwest Analog & Digital, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Midwest Analog & Digital, Inc.'s devices?
Among its 3 most recently registered devices, Midwest Analog & Digital, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Midwest Analog & Digital, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Midwest Analog & Digital, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Midwest Analog & Digital, Inc. in the registry?
The most recently registered devices listed for Midwest Analog & Digital, Inc. include ARRHYTHMIA PROGRAM MODULE, RECORDER, STRIP CHART WITH PRINTER and BEDSIDE PATIENT MONITOR W/MODULES.