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

GXY 1979-03-27

ELECTRODE, ELECTROFLEX

Applicant Andover Medical, Inc.

K-Number K790316

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BZW 1979-03-27

ARGYLE ESOPHAGEAL STETHOSCOPE

Applicant Sherwood Medical Industries

K-Number K790523

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DTM 1979-03-27

INTERSEPT* BLOOD FILTER W/ TUBING BYPASS

Applicant Surgikos, Inc.

K-Number K790435

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DPS 1979-03-27

META III

Applicant Hittman Medical Systems

K-Number K790300

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FHS 1979-03-26

DIALYZER, CD-800 COIL

Applicant Travenol Laboratories, S.A.

K-Number K790223

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IZL 1979-03-26

PORTABLE X-RAY UNIT

Applicant General X-Ray, Inc.

K-Number K790443

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KRH 1979-03-26

MERSILENE SUTURES

Applicant Hancock Laboratories, Inc.

K-Number K790534

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IZL 1979-03-26

PORTABLE X-RAY UNIT, MATRIX S GX-101

Applicant General X-Ray, Inc.

K-Number K790393

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GAA 1979-03-26

BURRON VENTED NEEDLE

Applicant National Patent Development Corp.

K-Number K790472

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MMK 1979-03-26

ANCHOR BRAND COUNT-TAINER

Applicant Anchor Products Co.

K-Number K790405

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IYX 1979-03-26

MULTIPLE PINHOLE TOMOGRAPHIC COLLIMOTER

Applicant Engineering Dynamics Corp.

K-Number K790499

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IZL 1979-03-26

MOBILE X-RAY UNIT

Applicant General X-Ray, Inc.

K-Number K790511

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