Burdick Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 44
What Burdick Corp. makes
Burdick Corp. manufactures medical devices for cardiac monitoring, exercise stress testing, and patient telemetry. Their portfolio includes electrocardiographs (e.g., E550, E560, EK-6), treadmill stress exercise systems, and central monitoring systems for real-time patient data acquisition. Additional products include treadmill controllers (e.g., M300 Monitor/Controller), ambulatory heart rate monitors (e.g., CSS-60), and telemetry systems for multi-channel ECG transmission.
The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory clearance via the 510(k) pathway. Products are listed in the FDA’s 510(k) database, reflecting compliance with U.S. medical device regulations. Burdick Corp. is headquartered in the United States.
Catalogue
Search and filter all 44 devicesFrequently asked questions
How many devices does Burdick Corp. have in the registry?
The registry currently lists 44 devices for Burdick Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Burdick Corp.'s devices?
Among its 44 most recently registered devices, Burdick Corp. has devices listed in FDA 510(k) (44 devices).
What risk classes do Burdick Corp.'s devices fall under?
Among its 44 most recently registered devices, the classes recorded for Burdick Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Burdick Corp. in the registry?
The most recently registered devices listed for Burdick Corp. include CENTRAL MONITORING SYSTEM, M300 MONITOR/CONTROLLER T500 TREADMILL, E550 ELECTROCARDIOGRAPH and ERGOMED 840/ERGOMED 840L.