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

DIF 1983-05-27

LIQUI-SERA ANTICONVULSANTS CONTROLS

Applicant Biodiagnostic Intl

K-Number K831278

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KOD 1983-05-27

LATEX URINARY CATHETERS

Applicant Wayne Surgical Products

K-Number K831369

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JHJ 1983-05-27

PREGNA-CERT, SLIDE PREGNANCY TEST

Applicant Diagnostic Specialties

K-Number K831180

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KLS 1983-05-27

EMIT QST THEOPHYLLINE ASSAY

Applicant Syva Co.

K-Number K831272

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GAD 1983-05-27

ANVIL RETRACTOR

Applicant Twin City Surgical, Inc.

K-Number K830585

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KNT 1983-05-27

LEVIN TUBE

Applicant Medovations, Inc.

K-Number K830987

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N/A 1983-05-27

DIRECTIGEN NEISSERIA MENINGITIDIS

Applicant Bd Becton Dickinson Vacutainer Systems Preanalytic

K-Number K830646

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CJM 1983-05-27

COAT-A-COUNT NO-EXTRACTION ALDOSTERONE

Applicant Diagnostic Products Corp.

K-Number K831178

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DCN 1983-05-27

TESTCORP RA

Applicant Myo-Tronics Research, Inc.

K-Number K831364

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FAD 1983-05-27

BARD URETERAL STENT

Applicant C.R. Bard, Inc.

K-Number K823487

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KYP 1983-05-25

LOPEZ-HORN CARRIER

Applicant Chiron Vision Corp.

K-Number K831312

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DTZ 1983-05-25

WILLIAM HARVEY H-1700 ADULT BLOOD OXYG-

Applicant C.R. Bard, Inc.

K-Number K831122

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