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

DSH 1979-06-01

LIFEPAK 5 MONITOR, CASSETTE, #800923-01

Applicant Physio-Control Corp.

K-Number K790757

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EWO 1979-05-31

TRACOR MODEL RA-411 MICROPROCESSOR

Applicant Tracor Instruments, Inc.

K-Number K790903

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DSF 1979-05-31

LS-8 VISICORDER

Applicant Honeywell, Inc.

K-Number K790825

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GXY 1979-05-31

T.E.N.S.* SINGLE-USE ELECTRODE

Applicant 3M Company

K-Number K790850

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JXB 1979-05-31

DERMATOPHYTIN O

Applicant Diagnostica, Inc.

K-Number K790671

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JPK 1979-05-31

COAGULATION ARP

Applicant Helena Laboratories

K-Number K790826

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DPS 1979-05-31

SIEMENS CARDIOSTAT 701

Applicant Elmed, Inc.

K-Number K790794

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DXY 1979-05-31

CARDIAC PULSE GENERATOR, 16 SERIES

Applicant Telectronics, Inc.

K-Number K790867

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DRX 1979-05-31

LIFEPATCH ECG ELECTRODES

Applicant Physio-Control Corp.

K-Number K790959

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EAT 1979-05-31

PULPTESTER MODEL 2001

Applicant Analytic Technology

K-Number K790799

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EFB 1979-05-31

DENTAL HANDPIECE

Applicant Venture Technology, Inc.

K-Number K790601

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JWT 1979-05-31

ASPERGILLUS FUMIGATUS, ASPERGILLUS FLAVU

Applicant Diagnostica, Inc.

K-Number K790672

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