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

CKG 1983-04-27

ACTH RIA SYSTEM-DSI 2300

Applicant Diagnostic Systems Laboratories, Inc.

K-Number K830893

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FXP 1983-04-27

MICRO-MITT

Applicant CooperVision, Inc.

K-Number K830821

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LLL 1983-04-27

ENA TEST KIT SM & RNP AUTO ANTIBODY

Applicant Calbiochem-Behring Corp.

K-Number K831036

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FOZ 1983-04-27

I.V. CATHETER PLACEMENT UNIT POLYURETH

Applicant Critikon Company, LLC

K-Number K830972

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KEA 1983-04-27

I.E.C COLUMN

Applicant Berwick Medical Products, Inc.

K-Number K830918

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GXY 1983-04-26

ELECTRODE 3799

Applicant Medtronic Vascular

K-Number K831046

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JWH 1983-04-26

INSALL/BURSTEIN FIBER METAL CONDYLAR/KNE

Applicant Zimmer, Inc.

K-Number K830121

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N/A 1983-04-26

MODEL VPS VASCULAR PROFILE SYSTEM

Applicant Hoffrel Instruments, Inc.

K-Number K837282

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N/A 1983-04-22

X-RAY BEAM FILTER

Applicant Eastman Kodak Company

K-Number K837334

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N/A 1983-04-21

LASER PHOTOCOAGULATOR

Applicant Hgm, Inc.

K-Number K837306

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N/A 1983-04-21

POWERED MOBILE BASE FOR 200MM AND 300MM SIZE DETECTORS

Applicant General Electric Co.

K-Number K837354

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N/A 1983-04-21

UWE SUN STREAM UWE BERMUDA UWE SUPER NOVA AND UWE BRONZARETTE

Applicant Unterwasser-Electric GmbH

K-Number K837278

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