510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K926293Substantially Equivalent

Angiocor Sidehole Infusion Catheter

Angiocor, Great Neck NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K926293 is the FDA 510(k) clearance record for ANGIOCOR SIDEHOLE INFUSION CATHETER, a class II device, cleared for Angiocor on under FDA product code LJS (Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days). FDA records list one 510(k) clearance for Angiocor. As of , FDA records show no recalls naming K926293.

Clearance record

Decision date
Received
(448 days to decision)
Product code
LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
Regulation
21 CFR 880.5970
Device class
Class II
Review panel
General Hospital
Applicant
Angiocor 55 Northern Blvd., Suite 301, Great Neck NY
510(k) summary
Statement
Third party review
No

Clearances, product code LJS

Trailing 12 months
3 clearances under product code LJS in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LJS, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260