Hayes Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Hayes Products, Inc. makes
Hayes Products, Inc. manufactures single-use EKG and ECG electrodes, including pregelled disposable electrodes for monitoring and stress/emergency applications. These products are designed for temporary skin attachment during cardiac testing and patient monitoring.
The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The portfolio is listed in the FDA’s 510(k) database. The manufacturer operates from the United States.
Catalogue
Ekg Electrodes, Disposable Ref K781940
Regimes: 510(k) Registry: 510(k)Pregelled Disposable Eelctro. Series 600 Ref K791140
Regimes: 510(k) Registry: 510(k)Pregelled Disp. Ekg Monitoring Elect- Ref K771447
Regimes: 510(k) Registry: 510(k)Pregelled Disposable Ecg Electrodes Ref K791139
Regimes: 510(k) Registry: 510(k)Stress/Emergency Eelctrode Ref K790883
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hayes Products, Inc. have in the registry?
The registry currently lists 5 devices for Hayes Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hayes Products, Inc.'s devices?
Among its 5 most recently registered devices, Hayes Products, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Hayes Products, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Hayes Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hayes Products, Inc. in the registry?
The most recently registered devices listed for Hayes Products, Inc. include EKG ELECTRODES, DISPOSABLE, PREGELLED DISPOSABLE EELCTRO. SERIES 600, PREGELLED DISP. EKG MONITORING ELECT- and PREGELLED DISPOSABLE ECG ELECTRODES.