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

FMF 1982-09-28

ARTERIAL LINE KIT

Applicant Martell Medical Products, Inc.

K-Number K822760

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LBZ 1982-09-28

TDX QUINIDINE

Applicant Abbott Laboratories

K-Number K822653

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DYB 1982-09-28

PERCUTANEOUS CATHETER INTRODUCER SET

Applicant Vertex Medical Corp.

K-Number K822593

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DQO 1982-09-28

TEFLON PIGTAIL/PERCUTANEOUS CARDIOVAS

Applicant Vertex Medical Corp.

K-Number K822598

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EBD 1982-09-28

CONCLUDE COMPOSITE LUTING CEMENT

Applicant 3M Company

K-Number K822714

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DSI 1982-09-28

MULTIPLE LEAD ARRHYTHMIA MODULE

Applicant Marquette Electronics, Inc.

K-Number K822030

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LFB 1982-09-28

NASAL SEPTAL BUTTONS

Applicant Abco Dealers, Inc.

K-Number K822637

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JHI 1982-09-28

MODEL UCG ASSAY

Applicant Monoclonal Antibodies, Inc.

K-Number K822520

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DXT 1982-09-28

MARK V

Applicant Medrad, Inc.

K-Number K822536

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CAE 1982-09-28

RESCUER

Applicant Armstrong Ind., Inc.

K-Number K822727

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FFK 1982-09-28

LITHOTRIPTOR ELECTRODE 4.5F

Applicant Monaghan Medical Corp.

K-Number K822585

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FMF 1982-09-28

REPLAM HYDROXYAPATATITE

Applicant Replam Corp.

K-Number K822420

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