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

KKX 1980-01-11

STERILIZATION PROCESS/ABSORBENT TOWEL

Applicant Procter & Gamble Mfg. Co.

K-Number K792623

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KKX 1980-01-11

STERILIZATION PROCESS CHANGE BOUNDARY

Applicant Procter & Gamble Mfg. Co.

K-Number K792621

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BYT 1980-01-11

CAM-10 CUIRASS SHELL

Applicant Lifecare Services, Inc.

K-Number K792673

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KQJ 1980-01-11

THROMBOKINETIC FIBRINOGEN ASSAY

Applicant Bio/Data Corp.

K-Number K792563

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KTS 1980-01-11

CENTRIA-SET TYPE D(ANTI-SHEEP/GOAT)

Applicant Union Carbide Corp.

K-Number K792637

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CFR 1980-01-11

GLUCOSE (HEXOKINASE) REAGENT SET

Applicant Macomb Chemical Co.

K-Number K792532

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GOK 1980-01-11

RUBELISA TEST KIT

Applicant Microbiological Assoc.

K-Number K792133

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JOJ 1980-01-11

STERILIZATION PROCESS/ MAYO PAD

Applicant Procter & Gamble Mfg. Co.

K-Number K792624

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JMG 1980-01-11

TERRITIN RIA KIT

Applicant Bd Becton Dickinson Vacutainer Systems Preanalytic

K-Number K792588

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CHJ 1980-01-11

SANDARE CHLORIDE PROCEDURE

Applicant Sandare Chemical Co., Inc.

K-Number K792531

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FYA 1980-01-11

STERILIZATION PROCESS /USE GOWNS

Applicant Procter & Gamble Mfg. Co.

K-Number K792622

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CHH 1980-01-11

ACA HIGH DENSITY LIPOPROTEIN CHOLES.

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

K-Number K792509

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