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

CGJ 1980-01-21

CENTRIA FSH RIA

Applicant Union Carbide Corp.

K-Number K792233

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ION 1980-01-21

COLOR CODED PUTTY SOFT, REGULAR & FIRM

Applicant Fred Sammons, Inc.

K-Number K800017

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CKA 1980-01-21

ALT REAGENT

Applicant Gilford Diagnostics

K-Number K800038

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JKA 1980-01-21

BLOOD FLUID FILTERS

Applicant Dade, Baxter Travenol Diagnostics, Inc.

K-Number K792723

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JIX 1980-01-21

CESIUM DILUENT (1.5 MM/L)

Applicant Gilford Diagnostics

K-Number K800043

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JIX 1980-01-21

SODIUM/POTASSIUM 140/5 MEQ/L)

Applicant Gilford Diagnostics

K-Number K800041

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KIE 1980-01-21

LDC UVIII FIXED WAVELENGTH ULTRAVIOLET

Applicant Laboratory Data Control

K-Number K800047

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GMD 1980-01-21

CRYPTOCOCCUS NEOFORMANS ANTISERUM, LATEX

Applicant Meridian Diagnostics, Inc.

K-Number K792693

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IRO 1980-01-21

BK-5203 FACILITATION VIBRATOR ELECTRIC

Applicant Fred Sammons, Inc.

K-Number K800018

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CEM 1980-01-21

DUPONT ACA ION SELECTIVE ELECTRODE

Applicant E.I. Dupont DE Nemours & Co., Inc.

K-Number K800016

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JCC 1980-01-21

MOPSO BUFFER

Applicant Electrophoresis Corp. of America

K-Number K792574

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JIX 1980-01-21

SODIUM/POTASSIUM (100/100 MEQ/E)

Applicant Gilford Diagnostics

K-Number K800040

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