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

KEQ 1980-01-24

KOH MOUNTING FLUID W/GLYCEROL

Applicant Meridian Diagnostics, Inc.

K-Number K792709

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GGP 1980-01-24

HELENA FACTOR XII DEFICIENT

Applicant Helena Laboratories

K-Number K792656

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HYW 1980-01-24

PARA-PAK(WHEATLEY'S TRICHROME STAIN)

Applicant Meridian Diagnostics, Inc.

K-Number K792706

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GMK 1980-01-24

IMMUNODIFFUSION BAND INTENSIFYING FLUID

Applicant Meridian Diagnostics, Inc.

K-Number K792692

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BTT 1980-01-24

VENTILATOR SET

Applicant Abbott Laboratories

K-Number K800056

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JSJ 1980-01-24

CAMPY THIO

Applicant Remel Co.

K-Number K792676

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IFQ 1980-01-24

PARA-PAK PVA

Applicant Meridian Diagnostics, Inc.

K-Number K792714

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DHR 1980-01-24

NORMAL GLOBULIN REAGENT

Applicant Meridian Diagnostics, Inc.

K-Number K792697

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CAF 1980-01-24

NEBULIZER TUBING SET

Applicant Abbott Laboratories

K-Number K800083

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CBK 1980-01-24

VENTILATOR TEST LUNG

Applicant Bio-Med Devices, Inc.

K-Number K800125

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JZQ 1980-01-24

OUCHTERLONY AGAR PLATES

Applicant Meridian Diagnostics, Inc.

K-Number K792699

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GMK 1980-01-24

NEGATIVE CONTROL SERUM

Applicant Meridian Diagnostics, Inc.

K-Number K792694

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