510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K051494Substantially Equivalent

Medical Image Digitizer, Models Cdcr 5020S, Uccr7001 and Tccr 7001

Cr Tech, Ltd., Baltimore MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K051494 is the FDA 510(k) clearance record for MEDICAL IMAGE DIGITIZER, MODELS CDCR 5020S, UCCR7001 AND TCCR 7001, a class II device, cleared for Cr Tech, Ltd. on under FDA product code MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager)). FDA records list one 510(k) clearance for Cr Tech, Ltd. As of , FDA records show no recalls naming K051494.

Clearance record

Decision date
Received
(107 days to decision)
Product code
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)
Regulation
21 CFR 892.1680
Device class
Class II
Review panel
Radiology
Applicant
Cr Tech, Ltd. 914 W. Patapsco Ave., Baltimore MD
510(k) summary
Statement
Third party review
No

Clearances, product code MQB

Trailing 12 months
3 clearances under product code MQB in the twelve months to October 2026, June 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code MQB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20262
July 20261
August 20260
September 20260
October 20260