510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K251692Substantially Equivalent

Advanced Tissue Resection Device

Micro-Tech (Nanjing) Co., Ltd., Nanjing, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K251692 is the FDA 510(k) clearance record for Advanced Tissue Resection Device, a class II device, cleared for Micro-Tech (Nanjing) Co., Ltd. on under FDA product code FDI (Snare, Flexible). FDA records list 41 510(k) clearances for Micro-Tech (Nanjing) Co., Ltd., from to . As of , FDA records show no recalls naming K251692.

Clearance record

Decision date
Received
(264 days to decision)
Product code
FDI Snare, Flexible
Regulation
21 CFR 876.4300
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Micro-Tech (Nanjing) Co., Ltd. # 10 Gaoke Third Rd., Nanjing National Hi-Tech Industrial, Nanjing, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FDI

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