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

EOQ 1982-10-26

PENTAX BRONCHOFIBERSCOPE #FB-19E

Applicant Pentax Precision Instrument Corp.

K-Number K822844

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EJJ 1982-10-26

SPHEREX E.C.T.

Applicant Jeneric Ind.

K-Number K822951

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FMF 1982-10-26

DISPOSABLE MICRO-INFUSION SYSTEM

Applicant Orange Medical Instruments, Inc.

K-Number K822928

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CGI 1982-10-26

MICROMEDIC ESTRIOL RIA KIT

Applicant Micromedic Systems

K-Number K822578

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BXK 1982-10-22

LUNG DIFFUSION MIXTURE

Applicant Liquid Carbonic Corp.

K-Number K822764

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HPX 1982-10-22

PRE-SERT

Applicant Allergan, Inc.

K-Number K822706

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BXK 1982-10-22

CLINICAL GAS MIXTURE-FLAMMABLE

Applicant Liquid Carbonic Corp.

K-Number K822762

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BTT 1982-10-22

DUAL SERVO HEATED RESPIRATORY HUMIDIFIER

Applicant Fisher & Paykel Allied Products , Ltd.

K-Number K822816

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DAA 1982-10-22

ANAZYME ANA PEROXIDASE TEST SYSTEM

Applicant Clinical Sciences, Inc.

K-Number K822911

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BSO 1982-10-22

DNA MEDICAL DURACATH

Applicant Moorehead Hospital Products, Inc.

K-Number K822436

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EJH 1982-10-22

RX BIOCAST

Applicant Jeneric Ind.

K-Number K822948

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HQG 1982-10-22

SUNGLASS LENSES

Applicant ZEISS

K-Number K822573

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