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

DXY 1979-02-26

MINILITH AND MICROLITH

Applicant Cardiac Pacemakers, Inc.

K-Number K790276

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DSK 1979-02-23

DINAMAP MODELS 1160 AND 1165

Applicant Applied Medical Research

K-Number K782073

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DQK 1979-02-23

QUINTON STATUS 1000

Applicant Quinton, Inc.

K-Number K782072

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DRG 1979-02-23

TELEMETRY SYSTEM 315

Applicant Ge Medical Systems Information Technologies

K-Number K790144

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DSP 1979-02-23

INTRA-AORTIC BALLOON-PUMP

Applicant Avco Medical Products

K-Number K790241

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DQX 1979-02-23

MOVABLE CORE SAFETY GUIDE

Applicant Cordis Corp.

K-Number K790258

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JQW 1979-02-22

ACCESSORY KIT, CENTRIFICHEM

Applicant Union Carbide Corp.

K-Number K790041

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N/A 1979-02-22

NEPHROSS 11F100

Applicant Redy Laboratories

K-Number K790352

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IKW 1979-02-22

BK-5371 GAD-19-BOUT PERSONAL MOBIL AID

Applicant Fred Sammons, Inc.

K-Number K790173

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FMG 1979-02-22

3-WAY STOPCOCK

Applicant Medex, Inc.

K-Number K782168

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KKX 1979-02-22

DRAPE PACKS, SURGICAL GOWNS

Applicant Convertors

K-Number K790234

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JME 1979-02-22

RIA KIT, GLUCOSE

Applicant Serono Laboratories, Inc.

K-Number K782143

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