Diatek, Inc.
United StatesFDA applicant, unverified
- Devices
- 15
What Diatek, Inc. makes
Diatek, Inc. manufactures medical devices including intravenous infusion pumps (e.g., the Secura IV Volumetric Infusion Pump), enteral nutrition pumps (e.g., the Enteroport Nutrition Pump), thermometer systems (e.g., the Diatek 600 Thermometer System and Model 700 Thermometer), and replacement kits for medical connectors (e.g., the Diatek Connector Assembly Replacement Kit). The company also produces cannula-catheter sets (e.g., the Diatek Cannon-Cath series) and specialized trach-secure devices (e.g., the Martin Trach-Secure). Additional products include administration sets (e.g., Secura Set Primary and Secondary) and modifications for existing systems like the Arkive platform.
Diatek’s devices are classified under FDA Class II and are listed via 510(k) clearance. The company operates from the United States, with its products regulated under the U.S. Food and Drug Administration’s medical device authorities.
Catalogue
Search and filter all 15 devicesFrequently asked questions
How many devices does Diatek, Inc. have in the registry?
The registry currently lists 15 devices for Diatek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diatek, Inc.'s devices?
Among its 15 most recently registered devices, Diatek, Inc. has devices listed in FDA 510(k) (15 devices).
What risk classes do Diatek, Inc.'s devices fall under?
Among its 15 most recently registered devices, the classes recorded for Diatek, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diatek, Inc. in the registry?
The most recently registered devices listed for Diatek, Inc. include ARKIVE (TM), DIATEK CONNECTOR ASSEMBLY REPLACEMENT KIT (CARK), SECURA SET PRIMARY ADMIN. SET and DIATEK MODEL 700 THERMOMETER.