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

FPA 1979-01-17

FILTER FOR HYPERALIMENTATION SET

Applicant Travenol Laboratories, S.A.

K-Number K782134

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DLJ 1979-01-17

LIDOCAINE CALIBRATOR KIT

Applicant Vitek Systems, Inc.

K-Number K780731

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FRN 1979-01-17

CUTTER 888-00 INFUSION PUMP

Applicant Sigmamotor, Inc.

K-Number K782019

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JMG 1979-01-17

IRMA TEST, NORDICLAB FERRITIN

Applicant Nordiclab Intl.

K-Number K782157

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N/A 1979-01-17

PROTHESIS, METACARPAL

Applicant Cutter Laboratories, Inc.

K-Number K781937

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FRN 1979-01-17

INFUSION PUMP, MODEL 5000

Applicant Sigmamotor, Inc.

K-Number K782020

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CEO 1979-01-17

REAGENT SYSTEM, INORGANIC PHOSPHORUS

Applicant Sigma Chemical Co.

K-Number K781806

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GDY 1979-01-17

SPONGES, STANFORD STERILE LAP

Applicant Stanford Professional Products

K-Number K790050

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DTB 1979-01-15

LEAD, SUTURELESS MYOCARDIAL

Applicant Daig Corp.

K-Number K782087

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DRT 1979-01-15

PULSETAKER

Applicant Van, Cott, Bagley, Cornwall & Mccarth

K-Number K782131

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DQO 1979-01-15

POST EXTRA SYSTOLIC POTENTIATOR

Applicant Medrad, Inc.

K-Number K781819

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DTJ 1979-01-15

DISPOSABLE HOLDER FOR BIOPROSTHESIS

Applicant Edwards Laboratories

K-Number K790022

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