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

GDO 1979-06-05

REYNOLDS DOUBLE HEMOCLIP APPLIERS

Applicant Edward Weck, Inc.

K-Number K790990

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GBJ 1979-06-05

GORDON IVS INTRAVENOUS STABILIZER

Applicant Whitman Medical Corp.

K-Number K790946

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JHG 1979-06-05

FETAL MATURITY TEST PROCEDURE

Applicant Helena Laboratories

K-Number K790798

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DRT 1979-06-05

STRESS TESTING SYSTEM, MULTI-POSITION

Applicant Engineering Dynamics Corp.

K-Number K790544

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GAD 1979-06-05

CLAMP COVERS

Applicant Medi-Spec

K-Number K790952

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EJJ 1979-06-05

AMALCAP-NON-GAMMA-2

Applicant Vivadent (Usa), Inc.

K-Number K790874

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BZA 1979-06-05

TEE ADAPTER

Applicant Airlife, Inc.

K-Number K790887

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CAH 1979-06-05

TWO-WAY ANESTHESIA FILTER

Applicant Pharmaseal Div., Baxter Healthcare Corp.

K-Number K790896

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DTB 1979-06-04

LEADS, IMPLANTABLE CARDIAC PACEMAKERS

Applicant Oscor, Inc.

K-Number K782018

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FAP 1979-06-01

BROWNE MODEL UD-4DE

Applicant Browne Corp.

K-Number K790478

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DSH 1979-06-01

QUICKSCAN HOLTER II

Applicant Intl. Medical, Inc.

K-Number K790476

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DTB 1979-06-01

ENDOCARDIAL PACING LEAD, MODEL 476-01

Applicant Intermedics, Inc.

K-Number K790548

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