510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K833762Substantially Equivalent

Percutaneous Retrograde Nephrostomy

Vpi, Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K833762 is the FDA 510(k) clearance record for PERCUTANEOUS RETROGRADE NEPHROSTOMY, cleared for Vpi on under FDA product code LJE (Catheter, Nephrostomy). FDA records list 2 510(k) clearances for Vpi, from to . As of , FDA records show one recall naming K833762.

Clearance record

Decision date
Received
(107 days to decision)
Product code
LJE Catheter, Nephrostomy
Device class
Unclassified
Review panel
Unknown
Applicant
Vpi 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code LJE

Trailing 12 months

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

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