510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K811414Substantially Equivalent

Baim Coronary Sinus Flow Analyzer

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

K811414 is the FDA 510(k) clearance record for BAIM CORONARY SINUS FLOW ANALYZER, a class II device, cleared for Electro-Catheter Corp. on under FDA product code DXG (Computer, Diagnostic, Pre-Programmed, Single-Function). FDA records list 35 510(k) clearances for Electro-Catheter Corp., from to . As of , FDA records show no recalls naming K811414.

Clearance record

Decision date
Received
(24 days to decision)
Product code
DXG Computer, Diagnostic, Pre-Programmed, Single-Function
Regulation
21 CFR 870.1435
Device class
Class II
Review panel
Cardiovascular
Applicant
Electro-Catheter Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DXG

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