510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K942110Substantially Equivalent

Inject-Snare

Endovations, Reading PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K942110 is the FDA 510(k) clearance record for INJECT-SNARE, a class II device, cleared for Endovations on under FDA product code FDI (Snare, Flexible). FDA records list 38 510(k) clearances for Endovations, from to . As of , FDA records show no recalls naming K942110.

Clearance record

Decision date
Received
(164 days to decision)
Product code
FDI Snare, Flexible
Regulation
21 CFR 876.4300
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Endovations Hill And George Ave.S, Reading PA
510(k) summary
Statement
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