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Life Corporation

Also registered as Life Corp.

United Statesfrom the FDA registration address FDA establishment FEI 2183615

Devices
5
Registrations
FDA
FDA recalls
0

Catalogue5

Newest first, rows 1-5 of 5

  • Life Oxygenpac For Trained Medical Personnel Ref K910434

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Life O2 Ref K910201

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Life Oxygenpac 6/12 Lpm Ref K910435

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Life Corp. Oxygen Pac Ref K855092

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Life-02 (Non-Refillable Cylinder) Ref K910699

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

Company details

FDA FEI number
2183615
Address
2200 Principal Row, Orlando, FL, 32837

Frequently asked questions

How many devices does LIFE CORPORATION have in the registry?

The registry currently lists 5 devices for LIFE CORPORATION. Devices recorded under merged duplicate company entries are counted once.

Which registries list LIFE CORPORATION's devices?

Among its 5 most recently registered devices, LIFE CORPORATION has devices listed in FDA 510(k) (5 devices).

What risk classes do LIFE CORPORATION's devices fall under?

Among its 5 most recently registered devices, the classes recorded for LIFE CORPORATION's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from LIFE CORPORATION in the registry?

The most recently registered devices listed for LIFE CORPORATION include LIFE OXYGENPAC FOR TRAINED MEDICAL PERSONNEL, LIFE O2, LIFE OXYGENPAC 6/12 LPM and LIFE CORP. OXYGEN PAC.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.