Intl. Biomedics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Intl. Biomedics, Inc. makes
Intl. Biomedics, Inc. manufactures an ambulatory pH data recorder system for monitoring gastrointestinal function and an infant life support module designed for neonatal respiratory assistance.
The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Ambulatory Ph Data Recorder System, Aph-2000 Ref K882551
Regimes: 510(k) Registry: 510(k)Infant Life Support Module-20 Ref K854065
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intl. Biomedics, Inc. have in the registry?
The registry currently lists 2 devices for Intl. Biomedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intl. Biomedics, Inc.'s devices?
Among its 2 most recently registered devices, Intl. Biomedics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Intl. Biomedics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Intl. Biomedics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intl. Biomedics, Inc. in the registry?
The most recently registered devices listed for Intl. Biomedics, Inc. include AMBULATORY PH DATA RECORDER SYSTEM, APH-2000 and INFANT LIFE SUPPORT MODULE-20.