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

DXJ 1978-06-14

M. 1336S CATHODE-RAY TUBE DISPLAY

Applicant Hewlett-Packard Co.

K-Number K780782

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ESD 1978-06-14

MM-CE DM (BEHIND THE EAR)

Applicant Argosy Intl. (Usa), Inc.

K-Number K780921

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DZP 1978-06-14

DIAMOND STONES

Applicant Venture Technology, Inc.

K-Number K780864

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MNE 1978-06-14

PODIATRIC MATERIAL

Applicant Crown Delta Corp.

K-Number K780391

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DDC 1978-06-14

THYMUNE-T

Applicant Burroughs Wellcome Co.

K-Number K780874

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DTB 1978-06-14

L-12, L-21, AND L-22 ELECTRODES

Applicant Coratomic, Inc.

K-Number K780569

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JHI 1978-06-14

B-HCG-RIA

Applicant Nuclear Medical Systems, Inc.

K-Number K780679

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ESD 1978-06-14

M25 PP (BEHIND THE EAR)

Applicant Argosy Intl. (Usa), Inc.

K-Number K780919

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ESD 1978-06-14

MM-CE 11 (BEHIND THE EAR)

Applicant Argosy Intl. (Usa), Inc.

K-Number K780920

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EBF 1978-06-14

ESTIC MICROFILL

Applicant Degussa Dental, Inc.

K-Number K780833

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CDX 1978-06-14

T4-RIA KIT

Applicant Clinical Bioresearch

K-Number K780707

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JOD 1978-06-14

EXTRACORPEAL CARDIOTOMY BLOOD FILTER

Applicant Cobe Laboratories, Inc.

K-Number K780653

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