510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K023907Substantially Equivalent

Cordis Maxi Ld Large Diameter Balloon Dilatation Catheter, Cordis Maxi Ld Pta Balloon Dilation Catheter

Cordis US Corp., Warren NJ / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K023907 is the FDA 510(k) clearance record for CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER, CORDIS MAXI LD PTA BALLOON DILATION CATHETER, a class II device, cleared for Cordis Corp. on under FDA product code KNQ (Dilator, Esophageal). FDA records list 332 510(k) clearances for Cordis US Corp., from to . As of , FDA records show no recalls naming K023907.

Clearance record

Decision date
Received
(23 days to decision)
Product code
KNQ Dilator, Esophageal
Regulation
21 CFR 876.5365
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Cordis Corp. 7 Powderhorn Dr., Warren NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KNQ

Trailing 12 months

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

FDA records show no clearances under product code KNQ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KNQ, 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