510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K761339Substantially Equivalent

Radial Travel Spec. Procedures Table

Xre Corp., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K761339 is the FDA 510(k) clearance record for RADIAL TRAVEL SPEC. PROCEDURES TABLE, a class II device, cleared for Xre Corp. on under FDA product code IZZ (Table, Radiographic, Non-Tilting, Powered). FDA records list one 510(k) clearance for Xre Corp. As of , FDA records show no recalls naming K761339.

Clearance record

Decision date
Received
(9 days to decision)
Product code
IZZ Table, Radiographic, Non-Tilting, Powered
Regulation
21 CFR 892.1980
Device class
Class II
Review panel
Radiology
Applicant
Xre Corp. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code IZZ

Trailing 12 months

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

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