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

FPB 1979-11-13

BIOGUARD INFUSION LINE FILTER

Applicant United States Surgical, A Division of Tyco Healthc

K-Number K791822

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KDJ 1979-11-13

CYCLER SETS MOD. #5C4143, 5C4144, 5C4145

Applicant Travenol Laboratories, S.A.

K-Number K791899

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KOD 1979-11-13

NON-A-THERM

Applicant Labarge, Inc.

K-Number K792037

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ETL 1979-11-13

ATMOS ENT PATIENT CHAIR #1

Applicant Jedmed Instrument Co.

K-Number K791937

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KRI 1979-11-13

OXYGENATOR GAS LINE FILTER

Applicant Cardio Systems, Inc.

K-Number K792151

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GQN 1979-11-13

HSV BIO-BEAD SCREEN KIT

Applicant Litton Bionetics

K-Number K791614

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CDD 1979-11-13

CENTRIA VITAMIN B12 FOLATE RADIO SET

Applicant Ventrex Laboratories, Inc.

K-Number K791216

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DTB 1979-11-13

LIFELINE - ENDOCARDIAL PACING LEAD

Applicant Intermedics, Inc.

K-Number K792168

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JSS 1979-11-13

STREP-SPEC

Applicant Micro-Media Systems, Inc.

K-Number K791991

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LBS 1979-11-13

DADE HIGH DENSITY LIPOPROTEIN CHOLESTERO

Applicant Dade, Baxter Travenol Diagnostics, Inc.

K-Number K792183

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ETD 1979-11-13

POPE UMBRELLA TUBE

Applicant Xomed, Inc.

K-Number K791680

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CGN 1979-11-13

125 I FOLATE SOLID PHASE RADIOASSAY

Applicant Abbott Laboratories

K-Number K792167

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