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

KOC 1983-03-17

ASAHI HOLLOW FIBER KIDNEYS NR SERIES

Applicant Advocacy International, Ltd.

K-Number K830183

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JSC 1983-03-17

CHS

Applicant Dms Laboratories

K-Number K830437

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LDD 1983-03-17

THERACARD 400

Applicant Siemens Medical Solutions USA, Inc.

K-Number K823828

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DSI 1983-03-17

HEARTRATE PLUS ECG CARDULE #1918

Applicant Spacelabs, Inc.

K-Number K830306

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EBE 1983-03-17

JOHNSON & JOHNSON OPAQUE COLOR MODIFI

Applicant Johnson & Johnson Professionals, Inc.

K-Number K830491

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KLE 1983-03-17

MICRODAPT DENTAL RESTORATIVE BONDING

Applicant Johnson & Johnson Professionals, Inc.

K-Number K830387

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GDY 1983-03-17

FLORET VAGINAL PACKING/TAMPONS

Applicant Ritmed, Inc.

K-Number K830260

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KYZ 1983-03-17

CLEAN-FLUSH

Applicant Burron Medical Products, Inc.

K-Number K830572

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N/A 1983-03-17

TAURUS LS THREE-PHASE GENERATORS

Applicant Elscint, Inc.

K-Number K837179

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DXY 1983-03-17

COMMAND ULTRA II

Applicant Cardiac Pacemakers, Inc.

K-Number K830382

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N/A 1983-03-17

TOMAX LS-20

Applicant Elscint, Inc.

K-Number K837182

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KOD 1983-03-17

STERILE CATHERIZATION PROCEDURE TRAYS

Applicant Welcon, Inc.

K-Number K830359

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