510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K030662Substantially Equivalent

Pathway Access Sheath Catheter

Vertelink Corporation, Mission Viejo CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K030662 is the FDA 510(k) clearance record for PATHWAY ACCESS SHEATH CATHETER, a class II device, cleared for Vertelink Corporation on under FDA product code EZN (Dilator, Catheter, Ureteral). FDA records list 3 510(k) clearances for Vertelink Corporation, from to . As of , FDA records show no recalls naming K030662.

Clearance record

Decision date
Received
(184 days to decision)
Product code
EZN Dilator, Catheter, Ureteral
Regulation
21 CFR 876.5470
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Vertelink Corporation 27001 La Paz, Suite 312, Mission Viejo CA
510(k) summary
Statement
Third party review
No

Clearances, product code EZN

Trailing 12 months

FDA records hold no clearances under product code EZN in the trailing twelve months.

FDA records show no clearances under product code EZN in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EZN, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260