510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K250747Substantially Equivalent

Globe® Pulsed Field System

KARDIUM Inc., Burnaby, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K250747 is the FDA 510(k) clearance record for Globe® Pulsed Field System, a class II device, cleared for Kardium, Inc. on under FDA product code DQK (Computer, Diagnostic, Programmable). FDA records list 2 510(k) clearances for Kardium, Inc., from to . As of , FDA records show no recalls naming K250747.

Clearance record

Decision date
Received
(105 days to decision)
Product code
DQK Computer, Diagnostic, Programmable
Regulation
21 CFR 870.1425
Device class
Class II
Review panel
Cardiovascular
Applicant
Kardium, Inc. 8518 Glenlyon Pkwy., Burnaby, CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DQK

Trailing 12 months
25 clearances under product code DQK in the twelve months to October 2026, February 2026 the highest month at 5.
Show the numbers
Monthly 510(k) clearances under FDA product code DQK, trailing twelve months
MonthClearances
November 20250
December 20254
January 20262
February 20265
March 20260
April 20263
May 20261
June 20263
July 20264
August 20262
September 20261
October 20260