FDA 510(k) clearance · back to tracker

MEDVISION(TM) IMAGING SOFTWARE

Evergreen Technologies, Inc. cleared K924178 on 1993-02-02, decision: substantially equivalent

K-number

K924178

Sponsor

Evergreen Technologies, Inc.

Device

MEDVISION(TM) IMAGING SOFTWARE

Class

Class I

Decision

Substantially Equivalent

Decision date

1993-02-02

Product code

LMD

Advisory committee

Radiology

Medical specialty

Radiology

Regulation number

892.2020

Official FDA record

Open K924178on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

openFDA JSON

Raw record →

Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

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Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.