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

KIS 1980-10-31

FETAL BOVINE SERUM

Applicant S&S Biologicals

K-Number K802418

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JFP 1980-10-31

ICA1 IONIZED CALCIUM ANALYZER

Applicant The London Co.

K-Number K801848

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DQO 1980-10-31

STERI-SLEEVE

Applicant Cordis Corp.

K-Number K802629

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DFT 1980-10-31

GOAT ANTI-HUMAN IGM

Applicant Protos Laboratories

K-Number K802177

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DXY 1980-10-31

MICROTHIN-PI BIPOLAR PULSE GENERATOR

Applicant Cardiac Pacemakers, Inc.

K-Number K802410

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CED 1980-10-31

CENTRIFICHEM INORGANIC PHOSPHORUS

Applicant Union Carbide Corp.

K-Number K802420

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KSR 1980-10-31

GAMBRO HEMOFREEZE-BAG

Applicant Gambro, Inc.

K-Number K801082

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JDB 1980-10-31

DEPALMA ELBOW

Applicant Zimmer, Inc.

K-Number K801574

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KHQ 1980-10-31

T3 UPTAKE TEST SYSTEM

Applicant American Diagnostic Corp.

K-Number K802468

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KKX 1980-10-31

DISP. FENESTRATED SURG. DRAPE SHEETS

Applicant American Convertors Div., American Pharmaseal

K-Number K802359

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IQK 1980-10-31

LOW BACK POSTURE PILLOW

Applicant Body Therapeutics, Inc.

K-Number K802442

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IYM 1980-10-31

THERMOCOMP

Applicant Hospital Financial Corp.

K-Number K801553

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