510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K920200Substantially Equivalent

Ultra-Vision Detail Intensifying Screen

E.I. Dupont de Nemours & Co., Inc., Wilmington DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K920200 is the FDA 510(k) clearance record for ULTRA-VISION DETAIL INTENSIFYING SCREEN, a class I device, cleared for E.I. Dupont DE Nemours & Co., Inc. on under FDA product code EAM (Screen, Intensifying, Radiographic). FDA records list 253 510(k) clearances for E.I. Dupont DE Nemours & Co., Inc., from to . As of , FDA records show no recalls naming K920200.

Clearance record

Decision date
Received
(134 days to decision)
Product code
EAM Screen, Intensifying, Radiographic
Regulation
21 CFR 892.1960
Device class
Class I
Review panel
Radiology
Applicant
E.I. Dupont DE Nemours & Co., Inc. Du Pont-Bmp22/1152, Wilmington DE
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