510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K010252Substantially Equivalent

Magnum

Magnum Equipment LLC, Oklahoma City OK / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K010252 is the FDA 510(k) clearance record for MAGNUM, a class II device, cleared for Magnum Equipment LLC on under FDA product code JFB (Table, Physical Therapy, Multi Function). FDA records list one 510(k) clearance for Magnum Equipment LLC. As of , FDA records show no recalls naming K010252.

Clearance record

Decision date
Received
(90 days to decision)
Product code
JFB Table, Physical Therapy, Multi Function
Regulation
21 CFR 890.5880
Device class
Class II
Review panel
Physical Medicine
Applicant
Magnum Equipment LLC 7222 W. Melrose Ln., Oklahoma City OK
510(k) summary
Statement
Third party review
No

Clearances, product code JFB

Trailing 12 months

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

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