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

DHR 1979-03-15

RHEUMATELL

Applicant Central Biological Co.

K-Number K790351

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LAS 1979-03-15

EMIT-QUINIDINE CONTROL

Applicant Syva Co.

K-Number K790402

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DHC 1979-03-15

IIF-A-N-DNA TEST KIT

Applicant Medica Corp.

K-Number K790106

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CBT 1979-03-13

MONOJECT ARTERIAL BLOOD SAMPLING DEVICE

Applicant Sherwood Medical Industries

K-Number K790196

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JHS 1979-03-12

ACA CREATINE KINASE ISOENZYMES

Applicant E.I. Dupont DE Nemours & Co., Inc.

K-Number K790088

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JPA 1979-03-12

PLASMA, STANDARDIZED NORMAL

Applicant Dade, Baxter Travenol Diagnostics, Inc.

K-Number K790204

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JQX 1979-03-12

NEPHELOMETER, MIC-2000 LASER

Applicant Dynatech Corp.

K-Number K790103

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JHI 1979-03-12

CHORIC-SHURE

Applicant Nuclear Medical Laboratories, Inc.

K-Number K790138

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KNK 1979-03-12

URIC ACID, BOUND ENZYME

Applicant Technicon Instruments Corp.

K-Number K790092

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CBP 1979-03-12

ONE-WAY VALVE

Applicant Airlife, Inc.

K-Number K790151

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JJF 1979-03-12

REAGENT KIT, LANCER GLUCOSE

Applicant Sherwood Medical Industries

K-Number K790197

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DHC 1979-03-12

LUPO-TEC

Applicant Armkel, LLC

K-Number K782129

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