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

DXW 1980-02-11

INFRASONDE AUTO/INFLATOR ELEC. VIBRATOR

Applicant Sphygmetrics, Inc.

K-Number K800179

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GDX 1980-02-11

I.M. BLADES

Applicant Instrument Makar, Inc.

K-Number K800177

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JEC 1980-02-11

OXFORD EXTERNAL FIXATION SYSTEM

Applicant Downs Surgical , Ltd.

K-Number K800184

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JJQ 1980-02-11

MICRO ELISA MINI READER

Applicant Dynatech Laboratories, Inc.

K-Number K800057

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JIS 1980-02-11

PIPET CALIBRATION KIT

Applicant Streck Laboratories, Inc.

K-Number K800062

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GEI 1980-02-11

MODEL 807 SUCTION CAUTERY FINGER TIP

Applicant Malibu Laboratories

K-Number K800022

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HGP 1980-02-11

COROMETRICS-PUSH BUTTON SPIRAL ELECTRODE

Applicant Ge Medical Systems Information Technologies

K-Number K792669

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IYO 1980-02-11

COMBISON 200 & COMBISON 202

Applicant Kt Medical, Inc.

K-Number K800094

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KNG 1980-02-11

MINIFETON 200

Applicant Kt Medical, Inc.

K-Number K800098

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IYO 1980-02-11

COMBISON 100-MODEL 100 & 110

Applicant Kt Medical, Inc.

K-Number K800091

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KNG 1980-02-11

MGD-3

Applicant Kt Medical, Inc.

K-Number K800095

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KRH 1980-02-11

AMP DIRECT VASCULAR MONITORING SYSTEM

Applicant American Medical Products, Inc.

K-Number K792646

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