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

KOD 1979-01-22

CATHETER, AKRON FOLEY TEFLON

Applicant Latex Ind., Inc.

K-Number K781751

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ESD 1979-01-22

HEARING AID, MODEL AA

Applicant Dahlberg Electronics, Inc.

K-Number K782122

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CAP 1979-01-22

PRESSURE ALARM

Applicant Thompson Respiration Products, Inc.

K-Number K782174

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GEX 1979-01-22

LASER SYSTEM, SHARPLAN 791/HE, CO2

Applicant Laser Industries , Ltd.

K-Number K782030

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CCL 1979-01-18

MONITOR, OXYCHEK OXYGEN

Applicant Critikon Company, LLC

K-Number K782114

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GKT 1979-01-17

FILTER, EYRPUR DISPOSABLE LEUKOCITE

Applicant Metrix Teknika, Inc.

K-Number K781803

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CGX 1979-01-17

HILAR

Applicant Hi Chem, Inc.

K-Number K782094

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IZL 1979-01-17

GENERAL EQUIPMENT COVER

Applicant Contour Fabricators, Inc.

K-Number K782155

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FLL 1979-01-17

INDICATOR, BIPOLAR TEMPERATURE

Applicant Micronex, Inc.

K-Number K782043

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GGK 1979-01-17

REAGENT, LYSING AND HEMOGLOBIN

Applicant Dade, Baxter Travenol Diagnostics, Inc.

K-Number K782098

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FCE 1979-01-17

ADMINISTRATION SET, ENEMA

Applicant Kelsar Corp.

K-Number K790005

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GOL 1979-01-17

CORDIA R

Applicant Cordis Corp.

K-Number K780885

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