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Parema, Ltd.

United KingdomFDA applicant, unverified

Devices
1

Catalogue1

Newest first, rows 1-1 of 1

  • K-Band And K-Crepe Ref K926072

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

Frequently asked questions

How many devices does Parema, Ltd. have in the registry?

The registry currently lists 1 device for Parema, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Parema, Ltd.'s devices?

Among its 1 most recently registered device, Parema, Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Parema, Ltd.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Parema, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Parema, Ltd. in the registry?

The most recently registered devices listed for Parema, Ltd. include K-BAND AND K-CREPE.

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