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

DRT 1983-05-18

CABINET FOR MULTIPLE FUNCTION BLOCKS

Applicant Electronics For Medicine, Inc.

K-Number K830795

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BTA 1983-05-18

CONNECTING TUBES

Applicant Medovations, Inc.

K-Number K831007

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DXN 1983-05-18

NORELCO DELUXE DIGITAL BLOOD PRESSURE

Applicant North American Philips Corp.

K-Number K830685

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KRC 1983-05-18

PREP-CHECK

Applicant General Devices

K-Number K830876

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CDX 1983-05-18

COAT-A-COUNT NEONATAL T4 KIT RIA KIT

Applicant Diagnostic Products Corp.

K-Number K831107

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LFK 1983-05-18

MAHURKAR FEMORAL CATHETER

Applicant Quinton, Inc.

K-Number K830674

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N/A 1983-05-18

PULSE LAVAGE

Applicant Micro-Aire Surgical Instruments, Inc.

K-Number K831230

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JTY 1983-05-18

MODIFIED NEW YORK MEDIUM

Applicant Gibco Laboratories Life Technologies, Inc.

K-Number K831359

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FCI 1983-05-18

BIOPSY ATTACHMENT

Applicant Diasonics, Inc.

K-Number K831317

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KRC 1983-05-18

Z VIEW METER MODEL 300

Applicant Lintronics Industries, Inc.

K-Number K830823

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DXN 1983-05-18

NORELCO ELECTRONIC DIGITAL BLOOD PRESS

Applicant North American Philips Corp.

K-Number K830684

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HTY 1983-05-18

WIRE & STEINMAN PINS

Applicant Kirschner Medical Corp.

K-Number K831005

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