510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K925924Substantially Equivalent

Neal Wrist Cones

Neal & Assoc., Inc., Columbia MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925924 is the FDA 510(k) clearance record for NEAL WRIST CONES, a class I device, cleared for Neal & Assoc., Inc. on under FDA product code FMQ (Restraint, Protective). FDA records list 2 510(k) clearances for Neal & Assoc., Inc., from to . As of , FDA records show no recalls naming K925924.

Clearance record

Decision date
Received
(136 days to decision)
Product code
FMQ Restraint, Protective
Regulation
21 CFR 880.6760
Device class
Class I
Review panel
General Hospital
Applicant
Neal & Assoc., Inc. 6005 N. Gregory Dr., Columbia MO
510(k) summary
Summary
Third party review
No

Clearances, product code FMQ

Trailing 12 months

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

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