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

DGC 1981-07-10

VENTRE/SEP IGE RIA TEST SET

Applicant Ventrex Laboratories, Inc.

K-Number K811559

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JAD 1981-07-10

RADIATION BOLUS

Applicant Action Products, Inc.

K-Number K811528

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FRG 1981-07-10

STERI-LOK DUAL PURPOSE PACKAGING/8400

Applicant 3M Company

K-Number K811670

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KNK 1981-07-10

SELECT-A-FLOW

Applicant Wenmar Intl. Corp.

K-Number K811857

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CHH 1981-07-10

CHOLESTEROL DETERMINATION

Applicant Biorent Diagnostic, Inc.

K-Number K811760

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FPA 1981-07-10

I.V. ADMINISTRATION SET

Applicant Medisystems Corp.

K-Number K811837

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LHF 1981-07-10

LEKSELL STEREOACTIC SYSTEM

Applicant Downs Surgical , Ltd.

K-Number K811726

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DBF 1981-07-10

AUTOPAK-12 FERRITIN KIT

Applicant Micromedic Systems

K-Number K811808

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CEO 1981-07-10

KING DIAGNOSTICS PHOSPHORUS TEST

Applicant King Diagnostics, Inc.

K-Number K811749

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BZT 1981-07-10

HI-LO TEMP ESOPHAGEAL STETHOSCOPE

Applicant Mallinckrodt Critical Care

K-Number K811862

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GAA 1981-07-10

A.D.T. REUSABLE BONE MARROW NEEDLE

Applicant Lab Industries, Inc.

K-Number K811771

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HWQ 1981-07-10

SILASTIC TENDON PASSER H.P.

Applicant Dow Corning Corp. Healthcare Industries Materials

K-Number K811679

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