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Medical Research Laboratories, Inc.

United StatesFDA applicant, unverified

Devices
19

What Medical Research Laboratories, Inc. makes

Medical Research Laboratories, Inc. manufactures portable and emergency medical devices, including defibrillators (such as the PORTA PAK 90 and 450SLL), external cardiac pacing systems (e.g., JUMP START Model 970300), and blood pressure monitors. The company also produces portable intensive care units, transcutaneous electrical nerve stimulators, and modified neuroprobe systems for specialized medical applications.

The company’s devices are classified under FDA regulations as Class II and Class III, with most submissions recorded via the 510(k) pathway. These products are listed in the FDA’s 510(k) registry, reflecting their regulatory clearance status. The manufacturer is based in the United States.

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

Catalogue19

Newest first, rows 1-19 of 19

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  • Porta Pak 90 Ref K840900

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

  • Dpd Defibrillator Ref K952085

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

  • Porta Pulse Iii #D320 Ref K833751

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

  • Modification To Portable Intensive Care Unit Ref K983307

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

  • Mrl Blood Pressure Monitor Ref K885191

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

  • 450SLL Defibrillator Ref K874204

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

  • Jump Start, Model 970300 Ref K021168

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

  • Dpd Defibrillator Ref K930548

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

  • Transcutaneous Elect. Nerve Stimulator Ref K803247

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

  • Modified Mrl Neuroprobe System V Ref K884869

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

  • Portable Intensive Care Unit Ref K974034

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

  • Portable Intensive Care Unit Ref K012030

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

  • 360 Slx Advisory Defibrillator Ref K935922

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

  • Portable Instensive Care Unit Ref K010207

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

  • Mrl Oximeter Ref K882664

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

  • Mrl Pacette, 450SLL Ref K880932

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

  • Portable Intensive Care Unit, Model Pic Ref K000712

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

  • Aedefibrillator Ref K002232

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

  • Portable Intensive Care Unit Ref K012766

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

Rows 1-19 of 19

Frequently asked questions

How many devices does Medical Research Laboratories, Inc. have in the registry?

The registry currently lists 19 devices for Medical Research Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Medical Research Laboratories, Inc.'s devices?

Among its 19 most recently registered devices, Medical Research Laboratories, Inc. has devices listed in FDA 510(k) (19 devices).

What risk classes do Medical Research Laboratories, Inc.'s devices fall under?

Among its 19 most recently registered devices, the classes recorded for Medical Research Laboratories, Inc.'s devices are Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from Medical Research Laboratories, Inc. in the registry?

The most recently registered devices listed for Medical Research Laboratories, Inc. include PORTA PAK 90, DPD DEFIBRILLATOR, PORTA PULSE III #D320 and MODIFICATION TO PORTABLE INTENSIVE CARE UNIT.

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