Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K921446Substantially Equivalent

Hot or Cold Pack (Thermipaq)

Thermionics Corp., Springfield IL / Traditional, Substantially Equivalent

K921446 is the FDA 510(k) clearance record for HOT OR COLD PACK (THERMIPAQ), a class I device, cleared for Thermionics Corp. on under FDA product code IME (Pack, Hot Or Cold, Reusable). FDA records list one 510(k) clearance for Thermionics Corp. As of , FDA records show no recalls naming K921446.

Clearance record

Decision date
Received
(108 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
Thermionics Corp. 828 S. Second St., Springfield IL
510(k) summary
Statement
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