510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K926040Substantially Equivalent

Heli-Tech Retrieval Basket

Cape Tech Medical Products, Falmouth MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K926040 is the FDA 510(k) clearance record for HELI-TECH RETRIEVAL BASKET, a class II device, cleared for Cape Tech Medical Products on under FDA product code LQR (Dislodger, Stone, Biliary). FDA records list 3 510(k) clearances for Cape Tech Medical Products, from to . As of , FDA records show no recalls naming K926040.

Clearance record

Decision date
Received
(22 days to decision)
Product code
LQR Dislodger, Stone, Biliary
Regulation
21 CFR 876.5010
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Cape Tech Medical Products 23 Davedon Dr., Falmouth MA
510(k) summary
Summary
Third party review
No

Clearances, product code LQR

Trailing 12 months
1 clearance under product code LQR in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LQR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260