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

GDJ 1980-01-28

VESSEL OCCLUDER

Applicant Cordis Corp.

K-Number K800074

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ILJ 1980-01-28

HYDRO PULSE MASSAGE

Applicant Hydro-Pulse Research, Inc.

K-Number K792641

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FMH 1980-01-28

PARA-PAK CLEAN VIAL

Applicant Meridian Diagnostics, Inc.

K-Number K792710

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ION 1980-01-28

THE VARIABLE LOAD KENETIC ENERGIZER

Applicant W.F. Pogue

K-Number K792642

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EAP 1980-01-28

PORTARAY

Applicant Siemens Corp.

K-Number K792535

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JSJ 1980-01-28

CAMPY BLOOD AGAR

Applicant Regional Media Laboratories

K-Number K792674

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GCY 1980-01-28

DAVOL/ABAMSON SILICONE SUMP DRAIN

Applicant Davol, Inc.

K-Number K800081

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JDG 1980-01-28

HEXCEL FEMORAL COMPONENT HIP PROSTHESIS

Applicant Hexcel Medical

K-Number K800051

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GDY 1980-01-28

STANFORD STERILE LAP SPONGES

Applicant Lukens Corp.

K-Number K800102

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FLE 1980-01-28

STERILIZING CASE CAT. NO. 65199

Applicant Edward Weck, Inc.

K-Number K800080

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IYO 1980-01-28

HIGH RESOLUTION IMAGING SYSTEM

Applicant Unirad Corp.

K-Number K792638

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KNA 1980-01-28

STERILIZATION PROCESS/DBL. GRIP CORD CLP

Applicant Procter & Gamble Mfg. Co.

K-Number K792631

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