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

EFB 1979-11-27

LS-100

Applicant Midwest

K-Number K792302

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KRG 1979-11-27

OMNICOR PROGRAMMER MODEL 222C

Applicant Cordis Corp.

K-Number K791419

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DXY 1979-11-27

UNIFOCAL 3-2 MODELS UNIPOLAR & BIPOLAR

Applicant American Pacemaker Corp.

K-Number K792232

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CDX 1979-11-27

TETRABEAD - 125 T4 SOLID PHASE DIAG. KIT

Applicant Abbott Laboratories

K-Number K792188

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EFB 1979-11-27

MW-8000

Applicant Midwest

K-Number K792304

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BWF 1979-11-27

MODEL TM2-BEHIND-THE-EAR TINNITUS

Applicant Starkey Laboratories, Inc.

K-Number K792214

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CET 1979-11-27

HARLECO BRAND CLINICARD LIPASE TEST SET

Applicant Dade, Baxter Travenol Diagnostics, Inc.

K-Number K791922

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DHR 1979-11-27

CORDIA RF

Applicant Cordis Corp.

K-Number K792061

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ERL 1979-11-27

FISCH DRILL SYSTEM

Applicant Jedmed Instrument Co.

K-Number K792159

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GEI 1979-11-27

A.D.E. ASPEN DISPERSIVE ELECTRODE

Applicant Zimmer, Inc.

K-Number K792315

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FTL 1979-11-27

USHER'S MARLEX TUBULAR MESH

Applicant Davol, Inc.

K-Number K792281

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DXG 1979-11-27

VDC

Applicant Life Sciences Manufacturing, Inc.

K-Number K791756

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