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

KPS 1981-01-15

GE RT/PLAN MAGNETIC TAPE DRIVE OPTION

Applicant General Electric Co.

K-Number K802801

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FEH 1981-01-15

ACMI BIPOLAR HEMOSTATIC ELECTRODE

Applicant American Cystocope Makers, Inc.

K-Number K803214

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FYA 1981-01-15

IRRADIATED BOUNDARY DEVICES

Applicant The Buckeye Cellulose Corp.

K-Number K803158

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N/A 1981-01-15

CAPSULE DENTAL AMALGAM

Applicant Dentsply Intl.

K-Number K803269

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GDY 1981-01-15

GAUZE SPONGES

Applicant Abco Dealers, Inc.

K-Number K803188

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IYO 1981-01-15

MARK III ULTRASONIC SCANNING SYSTEM

Applicant Advanced Technology Laboratories, Inc.

K-Number K802437

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BYE 1981-01-15

POSITIVE END EXPIRATORY PRESSURE VALVE

Applicant Fraser Harlake, Inc.

K-Number K802943

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IME 1981-01-15

COLD/HOT PACK

Applicant W.G. Whitney Corp.

K-Number K803299

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EFQ 1981-01-15

GAUZE SPONGES

Applicant Worldwide Surgical Gauze

K-Number K803172

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KDC 1981-01-15

SURGITEK MEDI-LOOPS

Applicant Medical Engineering Corp.

K-Number K803156

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ESD 1981-01-14

POST-AURICULAR HEARING AID (#PE830)

Applicant Hc Electronics

K-Number K810030

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EBF 1981-01-14

VISIO-DISPERS

Applicant Espe-Premier Sales Co.

K-Number K803227

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