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

HXB 1980-10-31

SURGICAL KNIVES & PROBES

Applicant Eder Instrument Co, Inc.

K-Number K802479

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IWZ 1980-10-31

KODAK ORTHO L FILM

Applicant Eastman Kodak Company

K-Number K802171

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JJQ 1980-10-31

DRUG DETECTION SYSTEM

Applicant Syva Co.

K-Number K802619

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LCW 1980-10-31

ENDAB DIGITOXIN ENZYME IMMUNOASSAY KIT

Applicant Immunotech Corp.

K-Number K802461

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FWZ 1980-10-31

SURCAN KNEE HOLDING DEVICE

Applicant Bend Orthopedic & Fracture Clinic

K-Number K802558

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KHQ 1980-10-31

OREAI-Q-TU TEST

Applicant Organon, Inc.

K-Number K802464

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CAF 1980-10-31

MISTY NEBULIZER

Applicant Airlife, Inc.

K-Number K802477

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DIS 1980-10-31

EMIT-STM BARBITURATE ASSAY

Applicant Syva Co.

K-Number K802617

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DYG 1980-10-31

7FRENCH FLOW DIRECTED TRIPLE LUMEN CATH

Applicant Waters Assoc., Inc.

K-Number K802481

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JLW 1980-10-31

TSH RADIOIMMUNOASSAY KIT

Applicant American Diagnostic Corp.

K-Number K802467

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HST 1980-10-31

COTTRELL 90/90 BACKTRAC

Applicant Lossing Orthopedic, Inc.

K-Number K802555

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JHJ 1980-10-31

GESTATE SLIDE EIKEN KIT AGG. METHOD HUM

Applicant Syn-Kit, Inc.

K-Number K802450

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