Intl. Hospital Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Baker Intestinal Tube, Twin Cuff Ref K792333
Regimes: 510(k) Registry: 510(k)Redo Central Venous Catheter-Neonate Ref K841443
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intl. Hospital Products, Inc. have in the registry?
The registry currently lists 2 devices for Intl. Hospital Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intl. Hospital Products, Inc.'s devices?
Among its 2 most recently registered devices, Intl. Hospital Products, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Intl. Hospital Products, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Intl. Hospital Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intl. Hospital Products, Inc. in the registry?
The most recently registered devices listed for Intl. Hospital Products, Inc. include BAKER INTESTINAL TUBE, TWIN CUFF and REDO CENTRAL VENOUS CATHETER-NEONATE.