510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K942909Substantially Equivalent

Kodak Insight Twin-Load Insert

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

K942909 is the FDA 510(k) clearance record for KODAK INSIGHT TWIN-LOAD INSERT, a class I device, cleared for Eastman Kodak Company on under FDA product code EAM (Screen, Intensifying, Radiographic). FDA records list 291 510(k) clearances for Eastman Kodak Company, from to . As of , FDA records show no recalls naming K942909.

Clearance record

Decision date
Received
(38 days to decision)
Product code
EAM Screen, Intensifying, Radiographic
Regulation
21 CFR 892.1960
Device class
Class I
Review panel
Radiology
Applicant
Eastman Kodak Company 343 State St., Rochester NY
510(k) summary
Statement
Third party review
No

Clearances, product code EAM

Trailing 12 months

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

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