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Appro Healthcare, Inc.

United StatesFDA applicant, unverified

Devices
2

What Appro Healthcare, Inc. makes

Appro Healthcare, Inc. manufactures sterile, single-use preparation systems for intravenous administration, including administration sets and cartridge assemblies designed for drug compounding and delivery.

These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Prepare Administration Set Ref K023769

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Prepare Cartridge Ref K023890

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

Frequently asked questions

How many devices does Appro Healthcare, Inc. have in the registry?

The registry currently lists 2 devices for Appro Healthcare, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Appro Healthcare, Inc.'s devices?

Among its 2 most recently registered devices, Appro Healthcare, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Appro Healthcare, Inc.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Appro Healthcare, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Appro Healthcare, Inc. in the registry?

The most recently registered devices listed for Appro Healthcare, Inc. include PREPARE ADMINISTRATION SET and PREPARE CARTRIDGE.

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