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

GWQ 1979-09-12

MODEL EEG-4214 ELECTROENCEPHALOGRAPH

Applicant Nihon Kohden America, Inc.

K-Number K791233

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FLL 1979-09-12

TEMP-STIK MODEL #300

Applicant Temp-Stik Corp.

K-Number K791558

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DTB 1979-09-12

MODEL 482-01 BIPOLAR COAXIAL PACING LEAD

Applicant Intermedics, Inc.

K-Number K791378

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GEI 1979-09-12

MODEL E2515 ELECTROSURGICAL ACCESSORY

Applicant Valleylab, Inc.

K-Number K791639

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DXY 1979-09-12

MODEL 228-02 THINLITH II PACEMAKER, BIPO

Applicant Intermedics, Inc.

K-Number K791379

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GEI 1979-09-12

MODEL E2510 SURGISWITCH

Applicant Valleylab, Inc.

K-Number K791638

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DWS 1979-09-12

CARDIOVASCULAR INSTRUMENTS-VARIOUS

Applicant Edward Weck, Inc.

K-Number K791710

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KPR 1979-09-07

THE MTD VARA SET CASETTE HOLDER

Applicant Mtd, Inc.

K-Number K791374

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BTA 1979-09-07

SYSTEC 280 INTEGRATED SUCTION SYSTEM

Applicant Stryker Corp.

K-Number K791349

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KNX 1979-09-07

CONPHAR URINARY DRAINAGE BAG-2000ML

Applicant Conphar, Inc.

K-Number K791265

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DTB 1979-09-07

MEDTRONIC MODELS 69914/699OU

Applicant Medtronic Vascular

K-Number K791667

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KNX 1979-09-07

CONPHAR FEMALE CATHETER W/BAG-STERILE

Applicant Conphar, Inc.

K-Number K791252

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