DeviceClearance

DIGITAL RADIOGRAPHY MODEL CXDI-55G— 510(k) K091435

Substantially Equivalent

Canon, Inc.

FDA 510(k) clearance K091435 for DIGITAL RADIOGRAPHY MODEL CXDI-55G, Substantially Equivalent on 2009-05-29. Applicant: Canon, Inc.. Device class: 2.

Clearance details

Applicant
Canon, Inc.
Product code
Code MQB
Device class
Class 2
Regulation
21 CFR 892.1680
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Lake Success, NY, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code MQB

view all

More clearances from Canon, Inc.

view all

Recalls naming K091435

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K091435.

Data sourced from openFDA. This site is unofficial and independent of the FDA.