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

N/A 1983-03-17

EXOR LS-24

Applicant Elscint, Inc.

K-Number K837176

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KEP 1983-03-17

CLEARIUM, MOUNTING MEDIUM

Applicant Surgipath Medical Industries, Inc.

K-Number K830659

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HRX 1983-03-17

ESA ELECTROSURGICAL ARTHROSCOPY GENERA

Applicant Concept, Inc.

K-Number K830499

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N/A 1983-03-17

TREPHIX THREE PHSE GENERATORS AND EXONON SINGLE PHASE GENERATORS

Applicant Elscint, Inc.

K-Number K837180

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KDP 1983-03-17

CONTAINER W/PRIMING SOLUTION

Applicant American Hospital Supply Corp.

K-Number K830343

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DXY 1983-03-17

UNILITH PULSE GENERATOR VVI #7542

Applicant Ela Medical, Inc.

K-Number K830401

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IFP 1983-03-17

MILLONIG'S MODIFIED PHOSPHATE BUFFERED

Applicant Surgipath Medical Industries, Inc.

K-Number K830582

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IFP 1983-03-17

NEUTRAL BUFFERED FORMALIN 10%

Applicant Surgipath Medical Industries, Inc.

K-Number K830583

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EBF 1983-03-17

PRISMA-FINE

Applicant Dentsply Intl.

K-Number K830442

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KTN 1983-03-17

MONO SCREENING TEST

Applicant Tago, Inc.

K-Number K830531

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HAW 1983-03-17

MENISCECTOMY TRAY #9715

Applicant Concept, Inc.

K-Number K823424

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LFJ 1983-03-17

MCDLSCK 126 DOUBLE LUMEN SUBCLAVIAN-FEM

Applicant Medcomp

K-Number K830438

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