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

FMG 1980-01-16

TANDEM ASSEMBLED 3&4 WAY STOPCOCKS

Applicant Tronomed, Inc.

K-Number K792124

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KHQ 1980-01-16

T3 UPTAKE (T3U) REAGENTS

Applicant Dade, Baxter Travenol Diagnostics, Inc.

K-Number K792607

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JXG 1980-01-16

CSF-VENTRICULAR CATHETER, STANDARD DES

Applicant Pudenz-Schulte Medical Research Corp.

K-Number K792007

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KQC 1980-01-16

PONCEAU S STAIN SET

Applicant Electrophoresis Corp. of America

K-Number K792550

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FPX 1980-01-16

LEUKOCLIP POROS

Applicant Beiersdorf, Inc.

K-Number K792667

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JQN 1980-01-16

ELVI MUCAPROTEINS

Applicant Volu Sol Medical Industries

K-Number K792554

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KME 1980-01-16

STERILIZATION PROCESS/BABY BLANKET

Applicant Procter & Gamble Mfg. Co.

K-Number K792626

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JXG 1980-01-16

CSF-CARDIAC/PERITONEAL CATHETER

Applicant Pudenz-Schulte Medical Research Corp.

K-Number K792005

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EHD 1980-01-16

GENERAL ELECTRIC PANELIPSE LD

Applicant General Electric Co.

K-Number K792581

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KSI 1980-01-16

GAMMA ARACHIS HYPOGEA LECTIN

Applicant Gamma Biologicals, Inc.

K-Number K792583

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KGX 1980-01-16

LEUKOPOR

Applicant Beiersdorf, Inc.

K-Number K792666

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KMO 1980-01-11

STERILIZATION PROCESS/T-BINDER

Applicant Procter & Gamble Mfg. Co.

K-Number K792629

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