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

DII 1979-10-30

19091-XXXXX SER. OF GLASS CAPILLARY COL.

Applicant Hewlett-Packard Co.

K-Number K791893

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CDZ 1979-10-30

(125I) TESTOSTERONE KIT

Applicant Radioassay Systems Laboratories, Inc.

K-Number K791999

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ESD 1979-10-30

RIONET HEARING AID HI-60

Applicant Rion Acoustic Instruments, Inc.

K-Number K791884

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HKP 1979-10-30

OCUTOME MODEL 8000

Applicant Cooper Medical Devices Corp.

K-Number K791898

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ETF 1979-10-30

ATMOS ENT TREATMENT SYSTEM SERVANT 3

Applicant Jedmed Instrument Co.

K-Number K791934

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JSH 1979-10-30

PHENOL RED BROTH

Applicant Isle Media and Sterile Products, Inc.

K-Number K791941

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ITJ 1979-10-30

DELTA ROLLING SELF-LICKING WALKER

Applicant Staricat, Inc.

K-Number K792064

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ESD 1979-10-30

RIONET HEARING AID HB-32

Applicant Rion Acoustic Instruments, Inc.

K-Number K791876

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JIS 1979-10-30

URIC ACID STANDARD

Applicant Gilford Diagnostics

K-Number K792046

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BTO 1979-10-30

TRACHEOSTOMY CARE KIT

Applicant National Patent Development Corp.

K-Number K792069

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ETF 1979-10-30

ATMOS ENT CABINET PRACTICA 3

Applicant Jedmed Instrument Co.

K-Number K791935

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JFH 1979-10-30

PAP-CHECK RIA KIT

Applicant Serono Laboratories, Inc.

K-Number K792043

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