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Iomed, Inc.

United StatesFDA applicant, unverified

Devices
17

Catalogue17

Newest first, rows 1-17 of 17

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  • Phoresor Model PM2000 Ref K001410

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

  • Phoresor Ii, Model PM900 Ref K974855

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

  • Phoresor Ii Auto, Model PM800 Modification Ref K934335

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

  • Transq 2 Ref K914264

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

  • Champion Iontophoretic Drug Delivery Device Ref K063465

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

  • Rh-801/Gs Model Transq(R)1 Ref K932621

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

  • Rh-806, Model Transq Ref K925800

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

  • Iontophoresis Device, Modification Ref K914621

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

  • Rh-806/Gs Model Transq(R)2 Ref K932620

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

  • Iontophoresis Device - Electrode Rh 800 Ref K896444

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

  • Rh-900 Ref K031115

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

  • Rh-950 Ref K033192

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

  • Phoresor Ii, Model PM900 Ref K982668

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

  • TRANSQ3 Ref K001522

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

  • Rh-801, Model Transq Ref K925806

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

  • Mw-1000 Iontophoretic Drug Delivery Electrode Ref K060236

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

  • Transq Electrode Phoresor Ii Ref K954126

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

Rows 1-17 of 17

Frequently asked questions

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

The registry currently lists 17 devices for Iomed, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Iomed, Inc.'s devices?

Among its 17 most recently registered devices, Iomed, Inc. has devices listed in FDA 510(k) (17 devices).

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

Among its 17 most recently registered devices, the classes recorded for Iomed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Iomed, Inc. include PHORESOR MODEL PM2000, PHORESOR II, MODEL PM900, PHORESOR II AUTO, MODEL PM800 MODIFICATION and TRANSQ 2.

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