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

DQO 1982-01-29

CORONARY INFUSION KIT

Applicant Mallinckrodt Critical Care

K-Number K820001

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FEB 1982-01-29

KEY MED LEEDS ENDOSCOPE DISINFECTOR

Applicant Keymed, Inc.

K-Number K820152

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IOL 1982-01-29

SAS EDUCATIONAL CHART

Applicant Structural Analysis Systems, Inc.

K-Number K813485

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KNC 1982-01-29

O.N.A.T.

Applicant Latex Medical Devices, Inc.

K-Number K820175

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HGL 1982-01-29

BIO-DERM COUPLING LOTION

Applicant Whs Products, Inc.

K-Number K827885

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DXN 1982-01-29

DIGITAL BLOOD PRESSURE UNIT

Applicant Conphar, Inc.

K-Number K813385

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KTW 1982-01-29

HIP PIN

Applicant The Deca Co.

K-Number K813340

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DQR 1982-01-29

SUBCLAVIAN JUGULAR CATHETER SET

Applicant Luther Medical Products, Inc.

K-Number K820102

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CGX 1982-01-29

LIQUIZYME CREATININE REAGENT SET

Applicant Amresco, Inc.

K-Number K813560

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DRS 1982-01-29

ANESTHESIOLOGY DEVICES

Applicant Bentley Laboratories, Inc.

K-Number K820046

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EBF 1982-01-29

ESTILUX POSTERIOR XR

Applicant Kulzer, Inc.

K-Number K813568

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DQO 1982-01-29

PRESSURE INDICATOR-REGULATOR

Applicant Advanced Catheter Systems

K-Number K813577

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