Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k) Clearances

510(k) cleared devices tracked by MedTracker

DTB 1979-02-01

LIFELINE BIPOLAR PACING LEAD MOD. 466-01

Applicant Intermedics, Inc.

K-Number K781498

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DRX 1979-02-01

ELECTRODE SYSTEM, QUIK-PREP

Applicant Quinton, Inc.

K-Number K782079

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FMG 1979-02-01

MANIFOLD, DISPOSABLE 3 VALVE

Applicant Cordis Corp.

K-Number K790010

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DTB 1979-02-01

ENDOCARIDAL PACING LEAD UNIPOLAR 477

Applicant Intermedics, Inc.

K-Number K781525

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DTB 1979-02-01

LIFELINE PACING LEAD MODEL 465-01

Applicant Intermedics, Inc.

K-Number K781497

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BZA 1979-02-01

MASK INTULATION ADAPTOR

Applicant Airlife, Inc.

K-Number K790149

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HCY 1979-02-01

DISPOSABLE VACUUM CURETTE

Applicant British Marketing Ent., Ltd.

K-Number K790032

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CEM 1979-02-01

SERUM, POTASSIUM DETERMINATION OF

Applicant Fisher Scientific Co., LLC

K-Number K790018

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GAA 1979-02-01

NEEDLE, BLOOD COLLECTING

Applicant Jelco Laboratories

K-Number K790079

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JLW 1979-02-01

RIA KIT, IMMO PHASE

Applicant Corning Medical & Scientific

K-Number K781953

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BZA 1979-02-01

TRACH T ADAPTER

Applicant Airlife, Inc.

K-Number K790157

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JJA 1979-02-01

DIAGNOSTIC KIT, FERRITAB-FE-59

Applicant Leeco Diagnostics, Inc.

K-Number K782159

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