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Careside Hemotology, Inc.

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Devices
1

What Careside Hemotology, Inc. makes

Careside Hemotology, Inc. manufactures the Careside APTT, a device used for measuring activated partial thromboplastin time (APTT) in blood samples, commonly employed in coagulation testing and monitoring.

The Careside APTT is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Careside Aptt Ref K014028

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Careside Hemotology, Inc. have in the registry?

The registry currently lists 1 device for Careside Hemotology, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Careside Hemotology, Inc.'s devices?

Among its 1 most recently registered device, Careside Hemotology, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Careside Hemotology, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Careside Hemotology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Careside Hemotology, Inc. in the registry?

The most recently registered devices listed for Careside Hemotology, Inc. include CARESIDE APTT.

Generated automatically from registry data and not verified by a human reviewer.