510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K050272Substantially Equivalent

Cryomedical Instruments Cryo-Pac Systems

Cryomedical Instruments, Ltd., Mansfield, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K050272 is the FDA 510(k) clearance record for CRYOMEDICAL INSTRUMENTS CRYO-PAC SYSTEMS, a class II device, cleared for Cryomedical Instruments, Ltd. on under FDA product code GXH (Device, Surgical, Cryogenic). FDA records list one 510(k) clearance for Cryomedical Instruments, Ltd. As of , FDA records show no recalls naming K050272.

Clearance record

Decision date
Received
(48 days to decision)
Product code
GXH Device, Surgical, Cryogenic
Regulation
21 CFR 882.4250
Device class
Class II
Review panel
Neurology
Applicant
Cryomedical Instruments, Ltd. Grove Way, Mansfield, GB
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GXH

Trailing 12 months

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

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