510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K940442Substantially Equivalent

Mpr-814

Xri, Inc., Tustin CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K940442 is the FDA 510(k) clearance record for MPR-814, a class I device, cleared for Xri, Inc. on under FDA product code IYB (Tube Mount, X-Ray, Diagnostic). FDA records list one 510(k) clearance for Xri, Inc. As of , FDA records show no recalls naming K940442.

Clearance record

Decision date
Received
(128 days to decision)
Product code
IYB Tube Mount, X-Ray, Diagnostic
Regulation
21 CFR 892.1770
Device class
Class I
Review panel
Radiology
Applicant
Xri, Inc. 2882-A Walnut Ave., Tustin CA
510(k) summary
Statement
Third party review
No

Clearances, product code IYB

Trailing 12 months

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

FDA records show no clearances under product code IYB in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code IYB, 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