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

IYN 1980-09-26

AUTO SECTOR SCANNER

Applicant Unirad Corp.

K-Number K801655

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KKX 1980-09-26

BOUNDARY SINGLE-USE DRAPES

Applicant Procter & Gamble Mfg. Co.

K-Number K802192

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CDQ 1980-09-26

DATA-ZYME UREA NITROGEN REAGENT SET

Applicant Data Medical Associates, Inc.

K-Number K802061

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FIE 1980-09-26

HEMO-CATH II KIDNEY DIALYSIS CATHETER

Applicant Medical Components, Inc.

K-Number K801966

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KHP 1980-09-26

DUPONT ACALACTIC ACID (LA) TEST

Applicant E.I. Dupont DE Nemours & Co., Inc.

K-Number K802064

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EWO 1980-09-26

RION DIAGNOSTIC AUDIOMETER

Applicant Rion Acoustic Instruments, Inc.

K-Number K802207

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JQC 1980-09-26

CONICAL TIPPED CENTRIFUGE TUBE 15M

Applicant Scientific Specialties, Inc.

K-Number K802210

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FTY 1980-09-26

RHYTIDOMETER

Applicant Aztec Medical Products, Inc.

K-Number K801939

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BTM 1980-09-26

AULD BAGGER KIT

Applicant Modern Medical Systems Co.

K-Number K802081

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FMG 1980-09-26

STOPCOCK 2-WAY, 3-WAY & 4-WAY

Applicant Stanco Medical, Inc.

K-Number K802258

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HST 1980-09-26

PROT-A-TRAC

Applicant Robert I. Branick, M.D.

K-Number K802072

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DSI 1980-09-26

OXFORD INTENSIVE CARE PATIENT MON. SYS

Applicant Oxford Medilog, Inc.

K-Number K802033

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