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

HCC 1983-09-01

FEEDBACK EMG SYSTEM PE-020

Applicant Bio-Feedback Systems, Inc.

K-Number K832333

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JSD 1983-09-01

ROGOSA BROTH

Applicant Oxoid U.S.A., Inc.

K-Number K832310

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MBV 1983-09-01

POROCOAT FREEMAN/SAMUELSON TOTAL KNEE

Applicant Depuy, Inc.

K-Number K831441

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CEC 1983-09-01

CORNING MAGIC SINGLE STEP FREE T4

Applicant Corning Medical & Scientific

K-Number K832381

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DIP 1983-09-01

A-GENT PHERYTOIN

Applicant Abbott Laboratories

K-Number K832419

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CFE 1983-09-01

CARDIZYME PLUS LD #65094/93

Applicant Em Industries, Inc.

K-Number K832314

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CIG 1983-09-01

ACA TOTAL BILIRUBIN ANALYTICAL TEST PAK

Applicant E.I. Dupont DE Nemours & Co., Inc.

K-Number K832357

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BZK 1983-09-01

OHIO 5400 VOLUME MONITOR

Applicant Airco/Ohio Medical Products

K-Number K832565

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KNT 1983-09-01

VIVONEX TUNGSTEN TIP TUBE-TWISTED WIRE

Applicant Norwich Eaton Pharmaceuticals, Inc.

K-Number K831971

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GTY 1983-09-01

PHADEBACT STREP POSITIVE CONTROLS

Applicant Pharmacia, Inc.

K-Number K832248

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IME 1983-08-31

NICE PACK

Applicant Universal Medical Instrument Corp.

K-Number K832193

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EJS 1983-08-31

X-704

Applicant Unitek Corp.

K-Number K832253

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