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

GAD 1979-12-05

AUTOMATIC RETRACTOR HOLDERS

Applicant Automated Medical Products, Inc.

K-Number K792145

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HSB 1979-12-05

CURVED KUNTSCHER INTRAMEDULLARY NAIL

Applicant Howmedica Corp.

K-Number K792203

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JDR 1979-12-05

HOWMEDICA COMPRESSION STAPLE SYSTEM

Applicant Howmedica Corp.

K-Number K792204

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DTX 1979-12-05

STANICOR, OMNI-STAN,MOD 333B,334A GAMMA

Applicant Cordis Corp.

K-Number K792348

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CAC 1979-12-05

ACU-MED RED MISER HEMOTHORAX BLOOD COLL.

Applicant Acumed Instruments Corp.

K-Number K791891

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JDZ 1979-12-05

HOWMEDICA MIX-KIT II

Applicant Howmedica Corp.

K-Number K792186

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KRA 1979-12-05

CONTINUOUS FLUSH DEVICE

Applicant Pharmaseal Div., Baxter Healthcare Corp.

K-Number K792141

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DTB 1979-12-05

IMPLANTABLE ENDOCARDIAL TINED ELECTRODE

Applicant Telectronics, Inc.

K-Number K792387

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ESD 1979-12-05

HEARING AID, UNITRON MODEL 905W

Applicant Unitron Industries, Inc.

K-Number K792237

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KXA 1979-12-05

TILLMAN HIP RESURFACING REPLACEMT PROS.

Applicant Waldemar Link GmbH & Co. KG

K-Number K792200

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DXH 1979-12-05

MEDTRONIC MODEL 9407 TELETRACE TRANSMITT

Applicant Medtronic Vascular

K-Number K792359

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FOG 1979-12-05

DISPOSA-HOOD

Applicant Utah Medical Products, Inc.

K-Number K792144

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