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

LFR 1979-08-03

KINETIC DETERMINATION OF UV GLUCOSE

Applicant The Dow Chemical Co.

K-Number K791110

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DRG 1979-08-03

KWIK-AWA VEST

Applicant Medical Specialties, Inc.

K-Number K791363

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CCL 1979-08-03

ANESTHESIA OXYGEN ANALYZER MODEL 101

Applicant Rule Medical Instruments, Inc.

K-Number K791199

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DXY 1979-08-03

ARCO PROGAMMABLE PACEMAKER SYSTEM

Applicant Arco Medical Products Co.

K-Number K791147

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JXG 1979-08-03

H-H SLOTTED VENTRICULAR CATHETER

Applicant Holter-Hausner Intl.

K-Number K791076

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FRL 1979-08-03

DEXIDE DISPOSABLE PREP PAD

Applicant Dexide, Inc.

K-Number K791167

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EBA 1979-08-03

PORCELIT

Applicant Harry J. Bosworth Co.

K-Number K790806

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KNT 1979-08-03

CONPHAR FEEDING TUBE-STERILE

Applicant Conphar, Inc.

K-Number K791257

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GWZ 1979-08-03

BUCKS NEUROLOGICAL HAMMER

Applicant Amdia Medical Products

K-Number K791336

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LCJ 1979-08-03

SUBCUTANEOUS TISSUE EXPANDER

Applicant Heyer Schulte Corp.

K-Number K790842

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KLK 1979-08-03

TCO2M MODEL 818

Applicant Novametrix Medical Systems, Inc.

K-Number K791152

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JPK 1979-08-03

PLATELET-CHEX PLUS

Applicant Streck Laboratories, Inc.

K-Number K791226

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