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

BYP 1979-05-21

AEROSOL MOUTHPIECE NO. M-091

Applicant Mem Medical, Inc.

K-Number K790932

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BYG 1979-05-21

OXYGEN BARB M-552

Applicant Mem Medical, Inc.

K-Number K790934

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CAF 1979-05-21

NEBULIZER NO. M-175

Applicant Mem Medical, Inc.

K-Number K790924

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BYX 1979-05-21

3-WAY T 22MM MALE

Applicant Mem Medical, Inc.

K-Number K790928

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GEI 1979-05-18

SAFETY HOLSTER, SINGLE-USE

Applicant Aspen Laboratories, Inc.

K-Number K790770

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ITG 1979-05-18

DELTA-LITE

Applicant Johnson & Johnson Professionals, Inc.

K-Number K790320

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FZT 1979-05-18

COLOR CODING OF SURGICAL INSTRUMENTS

Applicant Sara Dan, Inc.

K-Number K790684

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IMA 1979-05-18

STAO-HOTPACK

Applicant Staodynamics, Inc.

K-Number K790904

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DRX 1979-05-18

800 ECG ELECTRODE

Applicant Simonsen & Weels Eftf.

K-Number K790507

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DPS 1979-05-17

CARDIO-SLIDECOMP

Applicant Creative Instruments

K-Number K790869

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DZN 1979-05-17

ACCOR MATRIX

Applicant Accor, Inc.

K-Number K790633

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N/A 1979-05-17

CORRUGATED FLEXIBLE POLYETHYLENE

Applicant Airlife, Inc.

K-Number K790886

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