510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K810402Substantially Equivalent

Ace Cold Bandage

BD Becton Dickinson Vacutainer Systems Preanalytic, Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K810402 is the FDA 510(k) clearance record for ACE COLD BANDAGE, a class I device, cleared for Bd Becton Dickinson Vacutainer Systems Preanalytic on under FDA product code IME (Pack, Hot Or Cold, Reusable). FDA records list 632 510(k) clearances for Bd Becton Dickinson Vacutainer Systems Preanalytic, from to . As of , FDA records show no recalls naming K810402.

Clearance record

Decision date
Received
(14 days to decision)
Product code
IME Pack, Hot Or Cold, Reusable
Regulation
21 CFR 890.5700
Device class
Class I
Review panel
Physical Medicine
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code IME

Trailing 12 months

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

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