510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K161459Substantially Equivalent

Nexus DRTM Digital X-ray Imaging System (with PaxScan 4336Wv4)

Varian Medical Systems, X-Ray Products-Infimed, Liverpool NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K161459 is the FDA 510(k) clearance record for Nexus DRTM Digital X-ray Imaging System (with PaxScan 4336Wv4), a class II device, cleared for Varian Medical Systems, X-Ray Products-Infimed on under FDA product code MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager)). FDA records list 2 510(k) clearances for Varian Medical Systems, X-Ray Products-Infimed, from to . As of , FDA records show no recalls naming K161459.

Clearance record

Decision date
Received
(103 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
Varian Medical Systems, X-Ray Products-Infimed 121 Metropolitan Dr., Liverpool NY
510(k) summary
Summary PDF
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