510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K830696Substantially Equivalent

Venes Anti Embolism Stockings

Futuro Div. Jung Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K830696 is the FDA 510(k) clearance record for VENES ANTI EMBOLISM STOCKINGS, a class II device, cleared for Futuro Div. Jung Corp. on under FDA product code DWL (Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)). FDA records list 2 510(k) clearances for Futuro Div. Jung Corp., from to . As of , FDA records show no recalls naming K830696.

Clearance record

Decision date
Received
(24 days to decision)
Product code
DWL Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)
Regulation
21 CFR 880.5780
Device class
Class II
Review panel
General Hospital
Applicant
Futuro Div. Jung Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DWL

Trailing 12 months

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

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