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

EFQ 1980-01-09

TRACHEOTOMY SPONGE, W/NON-WOVEN NYLON

Applicant American Medical Disposable, Inc.

K-Number K792612

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ESD 1980-01-09

MODEL 341H (HEARING AID)

Applicant Telex Communications, Inc.

K-Number K792464

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EFQ 1980-01-09

CELLULOSE TRACHE SPONGE

Applicant American Medical Disposable, Inc.

K-Number K792615

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IWZ 1980-01-09

KODAK X-OMAT G FILM

Applicant Eastman Kodak Company

K-Number K792448

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JSG 1980-01-09

TODD HEWITT BROTH

Applicant Isle Media and Sterile Products, Inc.

K-Number K792423

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DXG 1980-01-09

CARDIAC OUTPUT COMPUTER, M-MLC-4100

Applicant Nihon Kohden America, Inc.

K-Number K792678

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DRN 1980-01-09

THE CIRCULATOR BOOT

Applicant Circulator Boot Corp.

K-Number K792354

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IWZ 1980-01-09

KODAK ORTHO G FILM

Applicant Eastman Kodak Company

K-Number K792293

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IWZ 1980-01-09

KODAK X-OMAT M20 PROCESSOR, MODEL 1

Applicant Eastman Kodak Company

K-Number K792435

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IMI 1980-01-09

DYNASOUND 601

Applicant Dynawave, Corp.

K-Number K791976

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EFQ 1980-01-09

TRACHOETOMY SPONGE, NON-ADHERENT CELL

Applicant American Medical Disposable, Inc.

K-Number K792614

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EFQ 1980-01-09

TRACHEOTOMY SPONGE, NON-ADHERENT W/HDPE

Applicant American Medical Disposable, Inc.

K-Number K792616

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