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

IWJ 1980-10-23

SCOTT NEEDLE & SCOTT MICK IMPLANTER

Applicant Mick Radio-Nuclear Instruments, Inc.

K-Number K801983

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BYI 1980-10-23

MODEL 2500 PNEUMATIC PERCUSSOR

Applicant Medical Equipment Development Co., Inc.

K-Number K802399

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FRN 1980-10-23

CORDIS DOW INFUSION PUMP

Applicant Cordis Corp.

K-Number K802301

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LEJ 1980-10-23

U.I. OCTOSON

Applicant Ausonics Pty , Ltd.

K-Number K801675

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CDD 1980-10-23

COMBOSTAT - NO-BOIL KIT

Applicant Ria Products, Inc.

K-Number K801578

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JWL 1980-10-23

FTA-ABS BIOPAK

Applicant Bioware Products

K-Number K802276

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KGZ 1980-10-23

ARROW CATHETER CLAMP

Applicant Arrow Intl., Inc.

K-Number K802367

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DTE 1980-10-23

EXTERNAL, TEMP. PORTABLE CARDIAC GENER

Applicant Telectronics, Inc.

K-Number K801953

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ODD 1980-10-23

E.R.C.P. CANNULA PRODUCT

Applicant Mill-Rose Laboratory

K-Number K802443

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LEJ 1980-10-23

JK INT'L, INC. SOLTRON UVA TANNING BED

Applicant Mottek Intl. Corp.

K-Number K802134

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JQP 1980-10-23

SP 120 SOPHISTICATE

Applicant Vickers America Medical Corp.

K-Number K802251

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IZL 1980-10-23

AMX-III

Applicant General Electric Co.

K-Number K802047

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