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 1978-01-30

TDL-100 B

Applicant Pacesetter Systems

K-Number K772050

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KPA 1978-01-30

AUTO. SLIDE STAINER

Applicant Honeywell, Inc.

K-Number K780017

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DXY 1978-01-30

PULSE GENERATOR, BIPOLAR, DEMAND

Applicant Cardiac Pacemakers, Inc.

K-Number K772241

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JXR 1978-01-30

SPECTROPHOTOMETER, MODEL 5000

Applicant The Perkin-Elmer Corp.

K-Number K780112

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DXY 1978-01-30

PULSE GENERATOR, BIPOLAR, PROGRAMMABLE

Applicant Cardiac Pacemakers, Inc.

K-Number K772239

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CDB 1978-01-30

17-HYDROXY TEST

Applicant Hycel, Inc.

K-Number K772426

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GBZ 1978-01-30

CATHETER, CHOLANGIOGRAM, OPERATIVE

Applicant Gesco Intl., Inc.

K-Number K772288

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DXY 1978-01-30

CARDIAC PACER, MODEL 208

Applicant Cordis Corp.

K-Number K780066

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JOJ 1978-01-30

ETHYLENE OXIDE STERILI. INDICATOR

Applicant Bio-Medical Sciences, Inc.

K-Number K772358

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HQG 1978-01-30

LENS, HARD RESIN

Applicant Borani Intl.

K-Number K772221

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DXY 1978-01-30

PULSE GENERATOR, UNIPOLAR, DEMAND

Applicant Cardiac Pacemakers, Inc.

K-Number K772240

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CCK 1978-01-30

ANALYZER-PLUG-IN, CO2 MODEL M 3104

Applicant Electronics For Medicine, Inc.

K-Number K780107

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