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

JXG 1979-01-15

CATHETERS, H-H VENTRICULAR

Applicant Holter-Hausner Intl.

K-Number K782105

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DXN 1979-01-11

AUTOMATIC BLOOD PRESSURE DEVICE

Applicant Welch Allyn, Inc.

K-Number K781517

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DJD 1979-01-10

ANALYTICAL TEST PACK, PRIMIDONE

Applicant E.I. Dupont DE Nemours & Co., Inc.

K-Number K781957

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JMF 1979-01-10

RIA TEST, NORDICALB HPL

Applicant Nordiclab Intl.

K-Number K782099

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JMG 1979-01-10

RIA KIT, FERRITIN SOLID PHASE

Applicant Bd Becton Dickinson Vacutainer Systems Preanalytic

K-Number K781946

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JJE 1979-01-10

ANALYZER ABA-200

Applicant Abbott Laboratories

K-Number K782014

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KJI 1979-01-10

RIA KIT, KANAMYCIN

Applicant Diagnostic Products Corp.

K-Number K782125

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CEW 1979-01-10

HORMONE KIT, PARATHYROID

Applicant Nichols Institute Diagnostics

K-Number K782010

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GEC 1979-01-10

BRUSH/SPONGE, DISPOSABLE

Applicant Dexide, Inc.

K-Number K782172

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FSE 1979-01-10

ARMBOARD CVER, DISPOSABLE

Applicant Anago, Inc.

K-Number K782092

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FFZ 1979-01-10

C-CORD

Applicant Concept, Inc.

K-Number K782046

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GEH 1979-01-10

CRYOSURGICAL DEVICE 2000

Applicant Valleylab, Inc.

K-Number K781956

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