Skip to content

Scientific & General Pty., Ltd.

Country not established

Devices
2

What Scientific & General Pty., Ltd. makes

Scientific & General Pty., Ltd. manufactures patient monitoring devices, including the HS7 and HS8 series, which are designed for real-time vital sign observation in clinical settings.

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

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

Catalogue2

Newest first, rows 1-2 of 2

  • Monitor HS7 Ref K782045

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Monitor HS8 Ref K782044

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

Frequently asked questions

How many devices does Scientific & General Pty., Ltd. have in the registry?

The registry currently lists 2 devices for Scientific & General Pty., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Scientific & General Pty., Ltd.'s devices?

Among its 2 most recently registered devices, Scientific & General Pty., Ltd. has devices listed in FDA 510(k) (2 devices).

What risk classes do Scientific & General Pty., Ltd.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Scientific & General Pty., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Scientific & General Pty., Ltd. in the registry?

The most recently registered devices listed for Scientific & General Pty., Ltd. include MONITOR HS7 and MONITOR HS8.

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