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

DTK 1977-06-22

VENA CAVA UMBRELLA FILTER, MODEL 7321

Applicant Edwards Laboratories

K-Number K771046

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KKX 1977-06-22

TRAY, IRRIGATION, STERILE, BASIC

Applicant Lukens Corp.

K-Number K770799

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CDP 1977-06-22

REAGENT, T-3 UPTAKE

Applicant G.D. Searle and Co.

K-Number K770738

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JJJ 1977-06-22

RADIOASSAY TUBES & RADIOASSAY TUBE CAPS

Applicant G.D. Searle and Co.

K-Number K770740

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EIC 1977-06-20

SYRINGE, ENDODONTIC, W/PERFORATED NEEDLE

Applicant National Patent Development Corp.

K-Number K770967

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DXY 1977-06-20

GENERATOR, PULSE, UNIPOLAR, #508

Applicant Cardiac Pacemakers, Inc.

K-Number K770880

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JEQ 1977-06-20

PRO-CARE

Applicant Young Dental Manufacturing Co. 1, LLC

K-Number K770997

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QJC 1977-06-20

DENTAL PLAQUE DISCLOSING AGENT

Applicant Evident Dental Co. , Ltd.

K-Number K770990

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KMJ 1977-06-20

PRESERVE LUBRICANT CODE NO. 43=4035

Applicant Codman & Shurtleff, Inc.

K-Number K770498

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DWS 1977-06-20

HUANG VEIN HOLDER, #21-8011

Applicant Codman & Shurtleff, Inc.

K-Number K771026

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HBA 1977-06-20

NEURO-SORB PATTIES

Applicant Instranetics, Inc.

K-Number K770894

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DXY 1977-06-20

GENERATOR, PULSE, BIPOLAR 3608

Applicant Cardiac Pacemakers, Inc.

K-Number K770881

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