510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K932342Substantially Equivalent

Model 500-6 Radiation Therapy Ionization Chamber

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

K932342 is the FDA 510(k) clearance record for MODEL 500-6 RADIATION THERAPY IONIZATION CHAMBER, cleared for Victoreen, Inc. on under FDA product code LNN. FDA records list 40 510(k) clearances for Victoreen, Inc., from to . As of , FDA records show no recalls naming K932342.

Clearance record

Decision date
Received
(213 days to decision)
Product code
LNN
Review panel
Unknown
Applicant
Victoreen, Inc. 6000 Cochran Rd., Cleveland OH
510(k) summary
Statement
Third party review
No

Clearances, product code LNN

Trailing 12 months

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

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