510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K252794Substantially Equivalent

Vision-MR™ Diagnostic Catheter

Imricor Medical Systems, Burnsville MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K252794 is the FDA 510(k) clearance record for Vision-MR™ Diagnostic Catheter, a class II device, cleared for Imricor Medical Systems, Inc. on under FDA product code DRF (Catheter, Electrode Recording, Or Probe, Electrode Recording). FDA records list 3 510(k) clearances for Imricor Medical Systems, Inc., from to . As of , FDA records show no recalls naming K252794.

Clearance record

Decision date
Received
(128 days to decision)
Product code
DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
Regulation
21 CFR 870.1220
Device class
Class II
Review panel
Cardiovascular
Applicant
Imricor Medical Systems, Inc. 400 Gateway Blvd., Burnsville MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DRF

Trailing 12 months
1 clearance under product code DRF 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 DRF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260