510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K842206Substantially Equivalent

Diaflex Nephrostomy Balloon Dilator

American Edwards Laboratories, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K842206 is the FDA 510(k) clearance record for DIAFLEX NEPHROSTOMY BALLOON DILATOR, a class II device, cleared for American Edwards Laboratories on under FDA product code EZN (Dilator, Catheter, Ureteral). FDA records list 89 510(k) clearances for American Edwards Laboratories, from to . As of , FDA records show no recalls naming K842206.

Clearance record

Decision date
Received
(120 days to decision)
Product code
EZN Dilator, Catheter, Ureteral
Regulation
21 CFR 876.5470
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
American Edwards Laboratories 803 N. Front St. Suite 3, Mchenry IL
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