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

JAK 1980-10-23

G.E. SCAN CAPABILITY CAT.#B7815F

Applicant General Electric Co.

K-Number K802045

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DLZ 1980-10-23

PHENOBARBITAL REAGENT TEST KIT

Applicant Beckman Instruments, Inc.

K-Number K802039

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EFN 1980-10-23

COTTON ROLLS

Applicant Worldwide Surgical Gauze

K-Number K802429

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JKA 1980-10-23

SERUM SEPARATOR

Applicant Scientific Specialties, Inc.

K-Number K802211

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DPS 1980-10-23

MODEL 633A THREE CHANNEL STRESS TEST

Applicant Quinton, Inc.

K-Number K802190

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JTN 1980-10-23

MINOCYCLINE 30MCG. SENSI DISC

Applicant Bd Becton Dickinson Vacutainer Systems Preanalytic

K-Number K802194

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DXN 1980-10-23

SD-700 BLOOD PRESSURE MONITOR

Applicant Industrial & Biomedical Sensors Corp.

K-Number K802201

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JHJ 1980-10-23

UCG-BETA SLIDE

Applicant Armkel, LLC

K-Number K802435

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GQH 1980-10-23

CMV TEST KIT

Applicant Immuno-Diagnostic Products, Inc.

K-Number K801963

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CDD 1980-10-23

VITAMIN B12 - NO-BOIL KIT

Applicant Ria Products, Inc.

K-Number K801579

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BWN 1980-10-23

THE IMMOBILIZER FOR OPEN & ARTHROSCOPIC

Applicant The Anspach Effort, Inc.

K-Number K802271

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IXC 1980-10-23

VIEW-LITE, MODEL-DL

Applicant Med-Western Electronics, Inc.

K-Number K802216

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