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Mcneil Healthcare LLC

Also registered as Mcneil Healthcare, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 1000305719

Devices
19
Registrations
FDA
FDA recalls
0

Catalogue19

Newest first, rows 1-19 of 19

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  • Non Adherent Dressing And Non Adherent Drain Dressing Ref K935930

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Post Op Sponge Ref K935937

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Conforming Roll Ref K935936

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Surgical Sponge X-Ray Detectable Ref K935993

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • X-Ray Packing Sponge Ref K935910

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Non Adherant Burn Pads Ref K935934

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Surgical Laparotomy Sponge X-Ray Detectable Ref K935942

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Burn Gauze Pads Ref K935935

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Ready Cut Gauze Gauze Bolts Ref K935941

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Gauze Fluff Ref K935939

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Gauze Sponge; Drain Sponge Ref K935940

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Bandage Rolls, Stretch Gauze Rolls, Textured Gauze Rolls Ref K935938

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Tonsil Sponges Ref K935882

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Non-Woven Sponge Ref K935931

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Specialty Sponges Ref K935881

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Packing Sponge Ref K935911

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Custom Burn Dressing Ref K935933

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Burn Compress Ref K935932

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Neurological Sponges Ref K935883

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

Rows 1-19 of 19

Company details

FDA FEI number
1000305719
Address
311 Rt 46 West, Fairfield, NJ, 07004

Frequently asked questions

How many devices does MCNEIL HEALTHCARE LLC have in the registry?

The registry currently lists 19 devices for MCNEIL HEALTHCARE LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list MCNEIL HEALTHCARE LLC's devices?

Among its 19 most recently registered devices, MCNEIL HEALTHCARE LLC has devices listed in FDA 510(k) (19 devices).

What risk classes do MCNEIL HEALTHCARE LLC's devices fall under?

Among its 19 most recently registered devices, the classes recorded for MCNEIL HEALTHCARE LLC's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from MCNEIL HEALTHCARE LLC in the registry?

The most recently registered devices listed for MCNEIL HEALTHCARE LLC include NON ADHERENT DRESSING AND NON ADHERENT DRAIN DRESSING, POST OP SPONGE, CONFORMING ROLL and SURGICAL SPONGE X-RAY DETECTABLE.

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.