510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K913425Substantially Equivalent

Dial-a-Rad Porta Rad Table

Dial-A-Rad, Orlando FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913425 is the FDA 510(k) clearance record for DIAL-A-RAD PORTA RAD TABLE, a class II device, cleared for Dial-A-Rad on under FDA product code IXQ (Table, Radiographic, Stationary Top). FDA records list one 510(k) clearance for Dial-A-Rad. As of , FDA records show no recalls naming K913425.

Clearance record

Decision date
Received
(481 days to decision)
Product code
IXQ Table, Radiographic, Stationary Top
Regulation
21 CFR 892.1980
Device class
Class II
Review panel
Radiology
Applicant
Dial-A-Rad P.O. Box 680823, Orlando FL
510(k) summary
Statement
Third party review
No

Clearances, product code IXQ

Trailing 12 months

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

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