510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K925721Substantially Equivalent

Kodak Ektascan Cp Primary High Freq. Vid.interface

Eastman Kodak Company, Rochester NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925721 is the FDA 510(k) clearance record for KODAK EKTASCAN CP PRIMARY HIGH FREQ. VID.INTERFACE, a class II device, cleared for Eastman Kodak Company on under FDA product code LMA (Digitizer, Image, Radiological). FDA records list 291 510(k) clearances for Eastman Kodak Company, from to . As of , FDA records show no recalls naming K925721.

Clearance record

Decision date
Received
(106 days to decision)
Product code
LMA Digitizer, Image, Radiological
Regulation
21 CFR 892.2030
Device class
Class II
Review panel
Radiology
Applicant
Eastman Kodak Company 343 State St., Rochester NY
510(k) summary
Summary
Third party review
No

Clearances, product code LMA

Trailing 12 months

FDA records hold no clearances under product code LMA in the trailing twelve months.

FDA records show no clearances under product code LMA in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LMA, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260