Intertech Resources, Inc.
United StatesFDA applicant, unverified
- Devices
- 29
What Intertech Resources, Inc. makes
Intertech Resources, Inc. manufactures single-use and reusable resuscitation and ventilation devices, including exhalation filters, manual resuscitators for adults and infants, and neonatal hyperinflation bag systems. Their portfolio also includes anesthesia breathing circuits, medication nebulizer kits, HEPA-filtered heat and moisture exchangers, and pediatric mouth-to-mask resuscitators. Additional products cover pressure-limiting elbows, disposable manometers, and specialized gas sampling lines for anesthesia machines.
The company’s devices are primarily classified as Class I or Class II under FDA regulations, with most requiring 510(k) clearance. These products are listed in the FDA’s 510(k) database, reflecting their regulatory status in the United States. The manufacturer operates from the US.
Catalogue
Search and filter all 29 devicesFrequently asked questions
How many devices does Intertech Resources, Inc. have in the registry?
The registry currently lists 29 devices for Intertech Resources, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intertech Resources, Inc.'s devices?
Among its 29 most recently registered devices, Intertech Resources, Inc. has devices listed in FDA 510(k) (29 devices).
What risk classes do Intertech Resources, Inc.'s devices fall under?
Among its 29 most recently registered devices, the classes recorded for Intertech Resources, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intertech Resources, Inc. in the registry?
The most recently registered devices listed for Intertech Resources, Inc. include RESUSCITATION BAG EXHALATION FILTER, 1ST RESPONSE DISPOSABLE MANOMETER, 1ST RESPONSE (TM) INFANT MANUAL RESUSCITATOR and INTERTECH NEWBORN HYPERINFLATION BAG SYSTEM.