510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K833779Substantially Equivalent

Yttro Filter

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

K833779 is the FDA 510(k) clearance record for YTTRO FILTER, a class II device, cleared for Yttro Corp. on under FDA product code IZW (Collimator, Automatic, Radiographic). FDA records list one 510(k) clearance for Yttro Corp. As of , FDA records show no recalls naming K833779.

Clearance record

Decision date
Received
(222 days to decision)
Product code
IZW Collimator, Automatic, Radiographic
Regulation
21 CFR 892.1610
Device class
Class II
Review panel
Radiology
Applicant
Yttro Corp. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code IZW

Trailing 12 months

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

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