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

DRT 1982-09-21

LIFE TRACE 40/42

Applicant Life Science Instrumentation, Inc.

K-Number K822389

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DXG 1982-09-21

STAT-SCAN

Applicant Survival Technology, Inc.

K-Number K822093

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DPS 1982-09-21

QUIKPAGE SCANNER

Applicant Agilent Technologies

K-Number K822582

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JSC 1982-09-21

WILKINS-CHALGREN ANAEROBE BROTH

Applicant Oxoid U.S.A., Inc.

K-Number K822665

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KPM 1982-09-21

DENVER PERITONEO-VENOUS SHUNT (DP-VS)

Applicant Denver Biomedicals, Inc.

K-Number K822686

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HGY 1982-09-21

LACT-ASSIST BREAST PUMP

Applicant Lact-Assist, Inc.

K-Number K822403

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CKA 1982-09-21

OPTIMIZED UV-GPT REAGENT SET

Applicant Biorent Diagnostic, Inc.

K-Number K822494

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BTI 1982-09-21

REPCO EASY-BREATHER CLINICAL AIR PUMP

Applicant Repcocarts USA, Inc.

K-Number K822512

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GEI 1982-09-21

POLYHESIVE PATIENT RETURN ELECTRODE

Applicant Valleylab, Inc.

K-Number K822572

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FMF 1982-09-17

NEEDLES(HYPODERMIC)

Applicant Impex Laboratories

K-Number K822534

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GGK 1982-09-17

CDL LYSING REAGENT

Applicant Connecticut Diagnostics, Ltd.

K-Number K822500

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DHN 1982-09-17

ANTINUCLEAR ANTOBODY CELL SUBSTRATE

Applicant Immulok, Inc.

K-Number K822607

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