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

CAC 1978-10-26

TRAUMA DRAINAGE SET 72T-32TTC

Applicant Sorensen Research

K-Number K781551

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DTM 1978-10-26

FILTER, ARTERIAL BLOOD W/TUBING BYPASS

Applicant Surgikos, Inc.

K-Number K781707

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CAC 1978-10-26

MEDIASTINAL DRAINAGE TUBE SET MDT-32TC2

Applicant Sorensen Research

K-Number K781552

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CAC 1978-10-26

MEDIASTINAL DRAINAGE TUBE SET MDT-36TC2

Applicant Sorensen Research

K-Number K781553

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FLN 1978-10-25

INTRA-ALERT

Applicant Pan-Tech Research, Inc.

K-Number K781297

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GES 1978-10-24

BLADE, 20 ANGLE/MICRO BLADE HOLDER

Applicant Edward Weck, Inc.

K-Number K781716

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N/A 1978-10-24

SODIUM CHLORIDE, 0.85%

Applicant Bioscientific

K-Number K781734

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EQN 1978-10-24

SHILEY CRICOTHYROTOMY TUBE

Applicant Shiley, Inc.

K-Number K781639

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FLE 1978-10-24

STERILIZER, EAGLE 2000

Applicant American Sterilizer Co.

K-Number K781684

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CIG 1978-10-24

BILIRUBIN DETERMINTAITON IN SERUM

Applicant Fisher Scientific Co., LLC

K-Number K781610

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JTZ 1978-10-24

MUELLER HINTON AGAR WITH 5% SHEEP BLOOD

Applicant Pittsburgh Micro-Media, Inc.

K-Number K780958

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HOX 1978-10-24

BAYLOW VISUAL ACUITY TESTER

Applicant Codman & Shurtleff, Inc.

K-Number K781452

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