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

KKX 1980-05-20

STERILE ABDOMINAL PAD

Applicant Medspec Corp.

K-Number K801068

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EHP 1980-05-20

VACUDENT LUMIX 70

Applicant Vacudent Sales Corp.

K-Number K800575

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GZT 1980-05-20

DISPOSABLE SKIN RETRACTOR

Applicant Cimarron Instruments, Inc.

K-Number K801151

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LBH 1980-05-20

PLY LESIVE

Applicant May-Pell Chemical Development Co.

K-Number K801047

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FYA 1980-05-20

WHITE KNIGHT DISP. STERILE BACK GOWN

Applicant G.D. Searle and Co.

K-Number K800927

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DGC 1980-05-20

125I-IGE RADIOIMMUNOASSAY KIT

Applicant Bio-Ria

K-Number K801019

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DXY 1980-05-20

MODEL 5985 PACEMAKER PULSE GENERATOR

Applicant Medtronic Vascular

K-Number K800285

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EGZ 1980-05-20

KWIX-BITE X-RAY FILM HOLDER

Applicant Henry Schein, Inc.

K-Number K801079

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FXP 1980-05-20

FLARE DIS. CONDUCTIVE&NON. SHOE COVERS

Applicant Flare Products, Inc.

K-Number K800809

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KKX 1980-05-20

WHITE KNIGHT SUPPLEMENTAL DRAPE

Applicant G.D. Searle and Co.

K-Number K800928

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KKX 1980-05-20

STERILE DRAPE 17X18 W/3 FENESTRATION

Applicant Veratex Corp.

K-Number K801033

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HSB 1980-05-20

KIRSCHNER WIRE

Applicant American Safety Equipment Corp.

K-Number K801010

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