510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K952233Substantially Equivalent

Clear-Pb Lead Plastic Overhead Barrier 56-628

Victoreen, Inc., Cleveland OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K952233 is the FDA 510(k) clearance record for CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628, a class I device, cleared for Victoreen, Inc. on under FDA product code EAK (Screen, Leaded, Operator Radiation Protector). FDA records list 40 510(k) clearances for Victoreen, Inc., from to . As of , FDA records show no recalls naming K952233.

Clearance record

Decision date
Received
(35 days to decision)
Product code
EAK Screen, Leaded, Operator Radiation Protector
Regulation
21 CFR 892.6500
Device class
Class I
Review panel
Radiology
Applicant
Victoreen, Inc. 6000 Cochran Rd., Cleveland OH
510(k) summary
Statement
Third party review
No

Clearances, product code EAK

Trailing 12 months

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

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