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

KCX 1978-01-03

DEPILATORY, ELECTRONIC

Applicant Dura Corp., The

K-Number K772322

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DZN 1978-01-03

MATRIX STRIP, DEAD-SOFT

Applicant Den-Mat Corp.

K-Number K772316

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EBZ 1978-01-03

FOTOFILL ACTIVATOR LIGHT

Applicant Johnson & Johnson Professionals, Inc.

K-Number K772278

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FKQ 1978-01-03

HEMODIALYSIS APPARATUS

Applicant Heald Manufacturing, Inc.

K-Number K772161

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FPA 1978-01-03

SCALP VEIN SETS

Applicant Suru Chemicals & Pharmaceuticals, Ltd.

K-Number K772008

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FKN 1978-01-03

A-V SHUNT EXTENSION

Applicant Quinton, Inc.

K-Number K771425

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HCZ 1978-01-03

MINICLAMPS, STABILIZ., FALLOPIAN TUBE

Applicant J. Sklar Mfg. Co., Inc.

K-Number K772229

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JEB 1978-01-03

ARTHROSTRESS

Applicant Mtd, Inc.

K-Number K772321

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EJH 1978-01-03

CROWN & BRIDGE ALLOY

Applicant Johnson & Johnson Professionals, Inc.

K-Number K772256

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KLC 1978-01-03

DENTAL CHAIR, VANGUARD

Applicant Ritter Co.

K-Number K772300

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KDJ 1978-01-03

RINSE BLOCK CONNECTOR

Applicant Quinton, Inc.

K-Number K771482

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CAC 1978-01-03

RECEPTAL ATS MEDIASTINAL LINER

Applicant Sorensen Research

K-Number K772280

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