510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K843533Substantially Equivalent

Cardiac Event Recorder

Cryo2 Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K843533 is the FDA 510(k) clearance record for CARDIAC EVENT RECORDER, a class II device, cleared for Cryo2 Corp. on under FDA product code DRT (Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)). FDA records list one 510(k) clearance for Cryo2 Corp. As of , FDA records show no recalls naming K843533.

Clearance record

Decision date
Received
(294 days to decision)
Product code
DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
Regulation
21 CFR 870.2300
Device class
Class II
Review panel
Cardiovascular
Applicant
Cryo2 Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DRT

Trailing 12 months
4 clearances under product code DRT in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DRT, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20261
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20261
October 20260