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

CAT 1979-05-17

NASAL, OXYGEN, CANNULA

Applicant Airlife, Inc.

K-Number K790885

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N/A 1979-05-17

CIRCUIT, BREATHING (W CONNEC, Y PIECE)

Applicant Airlife, Inc.

K-Number K790889

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EWO 1979-05-17

MIDDLE EAR ANALYZER (IMPED. AUDIOMTR)

Applicant Grason-Stadler, Inc.

K-Number K790846

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DTA 1979-05-17

CARDIOTEST 2200

Applicant Cardiac Pacemakers, Inc.

K-Number K790503

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N/A 1979-05-17

FACE TENT-VINYL

Applicant Airlife, Inc.

K-Number K790884

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KSF 1979-05-16

TEST CELLS

Applicant Hyland Therapeutic Div., Travenol Laboratories

K-Number K790249

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EBF 1979-05-16

FINESSE

Applicant L.D. Caulk Co.

K-Number K790585

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N/A 1979-05-16

MODEL H39C-BEHING-THE-EAR HEARING INSTRU

Applicant Marcon Hearing Instruments, Inc.

K-Number K790779

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DRS 1979-05-16

MICROTEC BACTERIAL FILTER

Applicant Medex, Inc.

K-Number K790407

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DSI 1979-05-16

ARRHYTHMIA II CARDULE

Applicant Spacelabs, Inc.

K-Number K790837

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EMA 1979-05-16

CHEMBOND

Applicant L.D. Caulk Co.

K-Number K790586

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EXD 1979-05-16

COLOSTOMY ENEMA DEVICE

Applicant Vabar Corp.

K-Number K790749

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