510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K230748Substantially Equivalent

Disposable Ureteral Access Sheath

Youcare Technology Co.,Ltd. (Wuhan), Wuhan, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K230748 is the FDA 510(k) clearance record for Disposable Ureteral Access Sheath, a class II device, cleared for Youcare Technology Co.,Ltd. (Wuhan) on under FDA product code FED (Endoscopic Access Overtube, Gastroenterology-Urology). FDA's definition for product code FED reads: "To facilitate passage and aid advancement of endoscopes into the body, especially in cases of repeated intubation". FDA records list 2 510(k) clearances for Youcare Technology Co.,Ltd. (Wuhan), from to . As of , FDA records show no recalls naming K230748.

Clearance record

Decision date
Received
(138 days to decision)
Product code
FED Endoscopic Access Overtube, Gastroenterology-Urology
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Youcare Technology Co.,Ltd. (Wuhan) Tangxunhu N. St., Wuhan, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FED

Trailing 12 months
5 clearances under product code FED in the twelve months to October 2026, September 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code FED, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20262
May 20260
June 20260
July 20260
August 20260
September 20263
October 20260