Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K935569Substantially Equivalent

Instant Hot or Cold Disposable Pack

CRYOPAK INDUSTRIES Inc., Canada, CA / Traditional, Substantially Equivalent

K935569 is the FDA 510(k) clearance record for INSTANT HOT OR COLD DISPOSABLE PACK, a class I device, cleared for Cryopak Industries, Inc. on under FDA product code IMD (Pack, Hot Or Cold, Disposable). FDA records list one 510(k) clearance for Cryopak Industries, Inc. As of , FDA records show no recalls naming K935569.

Clearance record

Decision date
Received
(109 days to decision)
Product code
IMD Pack, Hot Or Cold, Disposable
Regulation
21 CFR 890.5710
Device class
Class I
Review panel
Physical Medicine
Applicant
Cryopak Industries, Inc. P.O. Box 80807, Canada, CA
510(k) summary
Statement
Third party review
No

Clearances, product code IMD

Trailing 12 months

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

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