Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K861469Substantially Equivalent

Duthoy Stone Basket

Lake Region Mfg., Inc., Chaska MN / Traditional, Substantially Equivalent

K861469 is the FDA 510(k) clearance record for DUTHOY STONE BASKET, a class II device, cleared for Lake Region Mfg., Inc. on under FDA product code FFL (Dislodger, Stone, Basket, Ureteral, Metal). FDA records list 42 510(k) clearances for Lake Region Mfg., Inc., from to . As of , FDA records show no recalls naming K861469.

Clearance record

Decision date
Received
(23 days to decision)
Product code
FFL Dislodger, Stone, Basket, Ureteral, Metal
Regulation
21 CFR 876.4680
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Lake Region Mfg., Inc. 340 Lake Hazeltine Dr., Chaska MN
Third party review
No

Clearances, product code FFL

Trailing 12 months

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

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