510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K923584Substantially Equivalent

Therapax Dxt 300 Series 3

Oldelft Corp. of America, Fairfax VA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K923584 is the FDA 510(k) clearance record for THERAPAX DXT 300 SERIES 3, a class II device, cleared for Oldelft Corp. of America on under FDA product code JAD (System, Therapeutic, X-Ray). FDA records list 9 510(k) clearances for Oldelft Corp. of America, from to . As of , FDA records show no recalls naming K923584.

Clearance record

Decision date
Received
(179 days to decision)
Product code
JAD System, Therapeutic, X-Ray
Regulation
21 CFR 892.5900
Device class
Class II
Review panel
Radiology
Applicant
Oldelft Corp. of America 2735 Dorr Ave., Fairfax VA
510(k) summary
Statement
Third party review
No

Clearances, product code JAD

Trailing 12 months
1 clearance under product code JAD in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JAD, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260