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

DXG 1979-01-05

LVV OPTION

Applicant Honeywell, Inc.

K-Number K781855

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DSF 1979-01-05

WRITER, GEMINI-3

Applicant C-V Monitors Corp.

K-Number K781867

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DSF 1979-01-05

RECORDER, STRIP CHART WITH PRINTER

Applicant Midwest Analog & Digital, Inc.

K-Number K781873

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DRT 1979-01-04

MONITOR, HEART RATE MODEL 103

Applicant Roche Medical Electronics, Inc.

K-Number K782089

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CAZ 1979-01-04

TRAY, AUXILLARY BLOCK

Applicant Pharmaseal Div., Baxter Healthcare Corp.

K-Number K782069

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DRT 1979-01-04

MONITOR, HEART RATE MODEL 105

Applicant Roche Medical Electronics, Inc.

K-Number K782088

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DHN 1979-01-03

FIAX TEST KIT

Applicant Idt, A Division of Whittaker M.A. Bioproducts

K-Number K782041

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GKL 1979-01-03

HYCEL COUNTER 211

Applicant Hycel, Inc.

K-Number K782102

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JHO 1979-01-03

CHOLESTEROL REAGENT SUBSTRATE SET

Applicant Corning Medical & Scientific

K-Number K781970

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CIT 1979-01-03

AST

Applicant Gilford Diagnostics

K-Number K781784

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GKL 1979-01-03

HYCEL COUNTER 333

Applicant Hycel, Inc.

K-Number K782100

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CIG 1979-01-03

BILIRUBIN, DINGLE VALVE DPD

Applicant Boehringer Mannheim Corp.

K-Number K781921

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